acetylcarnitine has been researched along with Ovarian Neoplasms in 3 studies
Acetylcarnitine: An acetic acid ester of CARNITINE that facilitates movement of ACETYL COA into the matrices of mammalian MITOCHONDRIA during the oxidation of FATTY ACIDS.
Ovarian Neoplasms: Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS.
Excerpt | Relevance | Reference |
---|---|---|
"Peripheral neuropathy (PN) is a recognized side effect of microtubule-targeting agents and the most clinically relevant toxicity observed with the epothilone sagopilone (SAG)." | 2.78 | A double-blind, randomized phase II study to evaluate the safety and efficacy of acetyl-L-carnitine in the prevention of sagopilone-induced peripheral neuropathy. ( Baurain, JF; Berton-Rigaud, D; Campone, M; de Bont, N; Fabbro, M; Joly-Lobbedez, F; Pautier, P; Pinkert, J; Rolland, F; Schmelter, T; Stenzl, A; van Dijk, M, 2013) |
"Methods." | 2.78 | A double-blind, randomized phase II study to evaluate the safety and efficacy of acetyl-L-carnitine in the prevention of sagopilone-induced peripheral neuropathy. ( Baurain, JF; Berton-Rigaud, D; Campone, M; de Bont, N; Fabbro, M; Joly-Lobbedez, F; Pautier, P; Pinkert, J; Rolland, F; Schmelter, T; Stenzl, A; van Dijk, M, 2013) |
"OVCAR-3 and SKOV-3 ovarian cancer lines were incubated in ALCAR containing media." | 1.35 | Effect of acetyl-l-carnitine on ovarian cancer cells' proliferation, nerve growth factor receptor (Trk-A and p75) expression, and the cytotoxic potential of paclitaxel and carboplatin. ( Belisle, JA; Engle, DB; Gubbels, JA; Hutson, PR; Kushner, DM; Patankar, MS; Petrie, SE, 2009) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Campone, M | 1 |
Berton-Rigaud, D | 1 |
Joly-Lobbedez, F | 1 |
Baurain, JF | 1 |
Rolland, F | 1 |
Stenzl, A | 1 |
Fabbro, M | 1 |
van Dijk, M | 1 |
Pinkert, J | 1 |
Schmelter, T | 1 |
de Bont, N | 1 |
Pautier, P | 1 |
Engle, DB | 1 |
Belisle, JA | 1 |
Gubbels, JA | 1 |
Petrie, SE | 1 |
Hutson, PR | 1 |
Kushner, DM | 1 |
Patankar, MS | 1 |
Pisano, C | 1 |
Pratesi, G | 1 |
Laccabue, D | 1 |
Zunino, F | 1 |
Lo Giudice, P | 1 |
Bellucci, A | 1 |
Pacifici, L | 1 |
Camerini, B | 1 |
Vesci, L | 1 |
Castorina, M | 1 |
Cicuzza, S | 1 |
Tredici, G | 1 |
Marmiroli, P | 1 |
Nicolini, G | 1 |
Galbiati, S | 1 |
Calvani, M | 1 |
Carminati, P | 1 |
Cavaletti, G | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Preventive Effect of Acetyl-L-carnitine on Oxaliplatin-induced Peripheral Neuropathy: A Randomized, Controlled, Open-label, Phase 2 Trail[NCT05601479] | Phase 2 | 100 participants (Anticipated) | Interventional | 2022-11-01 | Not yet recruiting | ||
Multi-Center, Randomized, Double-Blind Active-Controlled, Parallel Group Study to Investigate Plasma Folate, Red Blood Cell Folate and Homocysteine Levels During a 24 Week Oral Administration of an OC Containing Folate Compared to OC Alone[NCT00468481] | Phase 3 | 385 participants (Actual) | Interventional | 2007-04-30 | Completed | ||
(REASON) Double-blind, Randomized Phase II Study to Evaluate the Safety and Efficacy of Acetyl-l-carnitine in the Prevention of Sagopilone-induced Peripheral Neuropathy.[NCT00751205] | Phase 2 | 150 participants (Actual) | Interventional | 2008-08-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: baseline and up to week 12
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 17.6 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 0.3 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: baseline and up to week 16
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 17.6 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 2.4 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: baseline and up to week 20
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 15.1 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | -1.6 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: baseline and up to week 4
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 15.2 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 0.6 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: baseline and up to week 8
Intervention | µg/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 18.4 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 2.2 |
Homocysteine concentrations in plasma were determined by Fluorescence Polarization Immunoassays (FPIA) using the Abbot AxSym analyzer in a clinical laboratory setting. (NCT00468481)
Timeframe: baseline and up to week 12
Intervention | µg/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | -0.3 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 0 |
Homocysteine concentrations in plasma were determined by Fluorescence Polarization Immunoassays (FPIA) using the Abbot AxSym analyzer in a clinical laboratory setting. (NCT00468481)
Timeframe: baseline and up to week 16
Intervention | µg/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | -0.2 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | -0.1 |
Homocysteine concentrations in plasma were determined by Fluorescence Polarization Immunoassays (FPIA) using the Abbot AxSym analyzer in a clinical laboratory setting. (NCT00468481)
Timeframe: baseline and up to week 20
Intervention | µg/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | -0.2 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | -0.2 |
Homocysteine concentrations in plasma were determined by Fluorescence Polarization Immunoassays (FPIA) using the Abbot AxSym analyzer in a clinical laboratory setting. (NCT00468481)
Timeframe: baseline and up to week 24
Intervention | µg/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | -0.3 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 0.1 |
Homocysteine concentrations in plasma were determined by Fluorescence Polarization Immunoassays (FPIA) using the Abbot AxSym analyzer in a clinical laboratory setting. (NCT00468481)
Timeframe: baseline and up to week 4
Intervention | µg/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 0 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 0 |
Homocysteine concentrations in plasma were determined by Fluorescence Polarization Immunoassays (FPIA) using the Abbot AxSym analyzer in a clinical laboratory setting. (NCT00468481)
Timeframe: baseline and up to week 8
Intervention | µg/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | -0.2 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 0 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: baseline and up to week 12
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 405.8 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 86.5 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: baseline and up to week 16
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 448.9 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 68.0 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: baseline and up to week 20
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 452.7 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 64.6 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: baseline and up to week 4
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 110.9 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | -37.6 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: baseline and up to week 8
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 310.3 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 68.2 |
The mean NTD risk reduction evaluated as the change from Baseline to Week 24 in NTD risk based on the formula of Daly et al (J Amer Med Assoc 1995;274(21):1698-702); NTD risk=exp (1.6463-1.2193 x natural log [RBC folate]) where natural log [RBC folate] is the natural log of RBC folate measured in nmol/L; Change from Baseline to Week 24 in NTD risk=NTD risk at Week 24 - NTD risk at Baseline (NCT00468481)
Timeframe: Baseline and week 24
Intervention | per 1000 birth (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | -0.51 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | -0.03 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: at baseline (week 0)
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 50.3 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 47.1 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 12
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 67.4 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 46.4 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 16
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 67.5 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 51.8 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 20
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 61.5 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 45.9 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 24
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 64.0 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 43.7 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 4
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 60.4 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 45.9 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 8
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 68.1 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 54.1 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: at baseline (week 0)
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 41.7 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 41.5 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 12
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 59.5 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 42.3 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 16
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 59.4 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 43.2 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 20
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 59.8 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 39.7 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 24
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 58.7 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 39.8 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 4
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 59.6 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 43.1 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: up to week 8
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 60.8 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 41.8 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: at baseline (week 0)
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1122.8 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1345.0 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 12
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1469.8 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1378.4 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 16
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1460.5 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1454.7 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 20
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1486.6 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1435.9 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 24
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1500.3 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1316.1 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 4
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1175.7 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1256.1 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 8
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1412.7 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1407.6 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: at baseline (week 0)
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 910.9 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 915.1 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 12
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1308.9 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1025.2 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 16
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1365.2 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 967.6 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 20
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1419.8 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 981.3 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 24
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1355.3 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 949.2 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 4
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1007.1 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 889.5 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: up to week 8
Intervention | nmol/L (Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1184.8 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 970.4 |
Folate concentrations in plasma were determined by an appropriately validated microbiological assay. (NCT00468481)
Timeframe: Week 24
Intervention | nmol/L (Least Squares Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 60.55 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 41.67 |
RBC folate=([whole blood folate*100]-[plasma folate*(100-hematocrit)])/hematocrit (NCT00468481)
Timeframe: Week 24
Intervention | nmol/L (Least Squares Mean) |
---|---|
Drospirenone (DRSP)/Ethinylestradiol (EE)/Metafolin (MTHF) | 1406.91 |
Drospirenone (DRSP)/Ethinylestradiol (EE) | 1022.21 |
1 trial available for acetylcarnitine and Ovarian Neoplasms
2 other studies available for acetylcarnitine and Ovarian Neoplasms
Article | Year |
---|---|
Effect of acetyl-l-carnitine on ovarian cancer cells' proliferation, nerve growth factor receptor (Trk-A and p75) expression, and the cytotoxic potential of paclitaxel and carboplatin.
Topics: Acetylcarnitine; Antineoplastic Combined Chemotherapy Protocols; CA-125 Antigen; Carboplatin; Cell G | 2009 |
Paclitaxel and Cisplatin-induced neurotoxicity: a protective role of acetyl-L-carnitine.
Topics: Acetylcarnitine; Animals; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Cell Survival; Cisplatin | 2003 |