pirenzepine has been researched along with Hyperlipemia in 7 studies
Pirenzepine: An antimuscarinic agent that inhibits gastric secretion at lower doses than are required to affect gastrointestinal motility, salivary, central nervous system, cardiovascular, ocular, and urinary function. It promotes the healing of duodenal ulcers and due to its cytoprotective action is beneficial in the prevention of duodenal ulcer recurrence. It also potentiates the effect of other antiulcer agents such as CIMETIDINE and RANITIDINE. It is generally well tolerated by patients.
Excerpt | Relevance | Reference |
---|---|---|
"Since their introduction to the US market, atypical antipsychotic drugs, such as olanzapine, have been widely prescribed for the management of psychosis and have increasingly been used in dermatologic settings for the treatment of psychogenic dermatoses." | 7.72 | Eruptive xanthomas associated with olanzapine use. ( Chang, HY; Hughes, E; Kimball, AB; Oro, AE; Ridky, TW, 2003) |
"Since their introduction to the US market, atypical antipsychotic drugs, such as olanzapine, have been widely prescribed for the management of psychosis and have increasingly been used in dermatologic settings for the treatment of psychogenic dermatoses." | 3.72 | Eruptive xanthomas associated with olanzapine use. ( Chang, HY; Hughes, E; Kimball, AB; Oro, AE; Ridky, TW, 2003) |
" However, accumulating evidence suggests that these agents, particularly clozapine and olanzapine, have serious side effects of their own, including weight gain and elevated glucose and triglyceride levels." | 3.71 | The effects of novel antipsychotics on glucose and lipid levels. ( Ballon, JS; Boyd, JA; Marder, SR; Meng, LR; Wirshing, DA; Wirshing, WC, 2002) |
" A small number of reports documenting modest hypertriglyceridemia related to newer antipsychotics have implicated fluperlapine, clozapine, and, most recently, olanzapine." | 3.71 | Novel antipsychotics and severe hyperlipidemia. ( Meyer, JM, 2001) |
"The degree of lipemia of each sample, indicated by turbidity, was ranked into categories from least to greatest and used for statistical analyses." | 1.32 | A study of matrix effects on an LC/MS/MS assay for olanzapine and desmethyl olanzapine. ( Chin, C; Karnes, HT; Zhang, ZP, 2004) |
"Risperidone was not associated with increased odds of hyperlipidemia compared with no antipsychotic exposure (OR, 1." | 1.31 | An assessment of the independent effects of olanzapine and risperidone exposure on the risk of hyperlipidemia in schizophrenic patients. ( Buchanan, RW; Fedder, DO; Koro, CE; Kreyenbuhl, J; L'Italien, GJ; Magder, LS; Revicki, D; Weiss, S, 2002) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 7 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Wirshing, DA | 1 |
Boyd, JA | 1 |
Meng, LR | 1 |
Ballon, JS | 1 |
Marder, SR | 1 |
Wirshing, WC | 1 |
Koro, CE | 1 |
Fedder, DO | 1 |
L'Italien, GJ | 1 |
Weiss, S | 1 |
Magder, LS | 1 |
Kreyenbuhl, J | 1 |
Revicki, D | 1 |
Buchanan, RW | 1 |
Landry, P | 1 |
Benaliouad, F | 1 |
Chang, HY | 1 |
Ridky, TW | 1 |
Kimball, AB | 1 |
Hughes, E | 1 |
Oro, AE | 1 |
Chin, C | 1 |
Zhang, ZP | 1 |
Karnes, HT | 1 |
Meyer, JM | 2 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Transcranial Magnetic Stimulation for Individuals With Tourette's Syndrome[NCT00529308] | Phase 2 | 20 participants (Actual) | Interventional | 2007-07-31 | Completed | ||
Aripiprazole for Clozapine Associated Medical Morbidity[NCT00345033] | Phase 4 | 38 participants (Actual) | Interventional | 2005-03-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
"The CGI-I is a clinician-rated scales that have been used in clinical trials for over 25 years. Clinicians rate patient improvement compared to baseline. By convention, 4 = No Change; scores of 5, 6, and 7 move in the direction of worsening; scores of 3, 2, and 1 correspond to Minimal Improvement, Much Improved or Very Much Improved, respectively. CGI-I ratings of Much or Very Much Improved at post-treatment are used to identify treatment responders." (NCT00529308)
Timeframe: 3 weeks
Intervention | participants (Number) |
---|---|
Active | 2 |
Sham | 8 |
"The CGI-I is a clinician-rated scales that have been used in clinical trials for over 25 years. Clinicians rate patient improvement compared to baseline. By convention, 4 = No Change; scores of 5, 6, and 7 move in the direction of worsening; scores of 3, 2, and 1 correspond to Minimal Improvement, Much Improved or Very Much Improved, respectively. CGI-I ratings of Much or Very Much Improved at post-treatment are used to identify treatment responders." (NCT00529308)
Timeframe: 3 weeks
Intervention | participants (Number) |
---|---|
Active | 1 |
Sham | 0 |
Motor Threshold (MT) is thought to be a measure of membrane excitability in pyramidal neurons. MT is defined as the minimum magnetic flux needed to elicit a threshold EMG response (50 µV in peak to peak amplitude) in a resting target muscle in 5 out of 10 trials using single pulse TMS administered to the contralateral primary motor cortex. MT for both right and left hand are determined, and the lowest is used to select the intensity for rTMS. (NCT00529308)
Timeframe: 3 weeks
Intervention | µV (Mean) |
---|---|
Active | 56.5 |
Sham | 63.8 |
Motor Threshold (MT) is thought to be a measure of membrane excitability in pyramidal neurons. MT is defined as the minimum magnetic flux needed to elicit a threshold EMG response (50 µV in peak to peak amplitude) in a resting target muscle in 5 out of 10 trials using single pulse TMS administered to the contralateral primary motor cortex. MT for both right and left hand are determined, and the lowest is used to select the intensity for rTMS. (NCT00529308)
Timeframe: 3 weeks
Intervention | µV (Mean) |
---|---|
Active | 56 |
Sham | 59.8 |
Y-GTSS is a clinician-rated scale used to assess tic severity. Motor and phonic tics are rated separately from 0 to 5 on several scales including number, frequency, intensity, complexity, and interference. Thus Motor and Phonic Tic scores can range from 0 to 25; the combined Total Tic Score ranges from 0 to 50. There is also an Impairment score that rates the overall burden due to tics. The Impairment scale yields a single score from 0 to 50 with higher scores indicating higher levels of overall impairment associated with tics. (NCT00529308)
Timeframe: 3 weeks
Intervention | units on a scale (Mean) |
---|---|
Active | 29.5 |
Sham | 31.5 |
A comparison between aripiprazole group and placebo group of change in Body Mass Index (BMI) measured at Baseline and Week 8. (NCT00345033)
Timeframe: Measured at Baseline and Week 8
Intervention | kg/m^2 (Mean) |
---|---|
Aripiprazole | -0.52 |
Placebo | 0.03 |
A comparison between the aripiprazole group and placebo group in change in glucose metabolism measured at Baseline and Week 8. (NCT00345033)
Timeframe: Measured at Baseline and Week 8
Intervention | min^-1 (Mean) |
---|---|
Aripiprazole | 0.003 |
Placebo | -0.005 |
A comparison between aripiprazole group and placebo group of change in insulin resistance measured at Baseline and Week 8. (NCT00345033)
Timeframe: Measured at Baseline and Week 8
Intervention | HOMA score (Mean) |
---|---|
Aripiprazole | 0.6 |
Placebo | 0.65 |
A comparison of aripiprazole group and placebo group in change in total cholesterol measured at Baseline and Week 8. (NCT00345033)
Timeframe: Measured at Baseline and Week 8
Intervention | mg/dL (Mean) |
---|---|
Aripiprazole | -15.3 |
Placebo | 5.6 |
(NCT00345033)
Timeframe: Measured at Baseline and Week 8
Intervention | mg/dL (Mean) |
---|---|
Aripiprazole | -5.9 |
Placebo | -7.3 |
A comparison between aripiprazole group and placebo group in change in weight measured at Baseline and Week 8. (NCT00345033)
Timeframe: Measured at Baseline and Week 8
Intervention | kg (Mean) |
---|---|
Aripiprazole | -1.5 |
Placebo | 0.3 |
7 other studies available for pirenzepine and Hyperlipemia
Article | Year |
---|---|
The effects of novel antipsychotics on glucose and lipid levels.
Topics: Antipsychotic Agents; Benzodiazepines; Blood Glucose; Body Mass Index; Cholesterol; Cholesterol, HDL | 2002 |
The effects of novel antipsychotics on glucose and lipid levels.
Topics: Antipsychotic Agents; Benzodiazepines; Blood Glucose; Body Mass Index; Cholesterol; Cholesterol, HDL | 2002 |
The effects of novel antipsychotics on glucose and lipid levels.
Topics: Antipsychotic Agents; Benzodiazepines; Blood Glucose; Body Mass Index; Cholesterol; Cholesterol, HDL | 2002 |
The effects of novel antipsychotics on glucose and lipid levels.
Topics: Antipsychotic Agents; Benzodiazepines; Blood Glucose; Body Mass Index; Cholesterol; Cholesterol, HDL | 2002 |
An assessment of the independent effects of olanzapine and risperidone exposure on the risk of hyperlipidemia in schizophrenic patients.
Topics: Adult; Adverse Drug Reaction Reporting Systems; Aged; Antipsychotic Agents; Benzodiazepines; Case-Co | 2002 |
Should lipids be monitored during the first year of treatment with an atypical antipsychotic?
Topics: Antipsychotic Agents; Benzodiazepines; Cholesterol; Clozapine; Humans; Hyperglycemia; Hyperlipidemia | 2003 |
Eruptive xanthomas associated with olanzapine use.
Topics: Adult; Antipsychotic Agents; Benzodiazepines; Female; Humans; Hyperlipidemias; Male; Middle Aged; Ol | 2003 |
A study of matrix effects on an LC/MS/MS assay for olanzapine and desmethyl olanzapine.
Topics: Anticoagulants; Benzodiazepines; Calibration; Chromatography, Liquid; Citrates; Edetic Acid; Heparin | 2004 |
Novel antipsychotics and severe hyperlipidemia.
Topics: Adolescent; Adult; Antipsychotic Agents; Benzodiazepines; Dibenzothiazepines; Female; Humans; Hyperl | 2001 |
A retrospective comparison of weight, lipid, and glucose changes between risperidone- and olanzapine-treated inpatients: metabolic outcomes after 1 year.
Topics: Adult; Aged; Anticonvulsants; Antipsychotic Agents; Benzodiazepines; Blood Glucose; Body Weight; Dia | 2002 |