clofibric acid has been researched along with Osteoporosis in 1 studies
Clofibric Acid: An antilipemic agent that is the biologically active metabolite of CLOFIBRATE.
clofibric acid : A monocarboxylic acid that is isobutyric acid substituted at position 2 by a p-chlorophenoxy group. It is a metabolite of the drug clofibrate.
Osteoporosis: Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Pahan, K | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Effect of a Nutritional Support System to Reduce Complications in Patients With Covid-19 and Comorbidities in Stage III[NCT04507867] | 80 participants (Actual) | Interventional | 2020-09-07 | Completed | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Total number of patients with gastrointestinal symptoms at the end of follow-up at day 40.Those symptoms perceived abdominal region (pain, burn, pressure, nausea, vomiting) (NCT04507867)
Timeframe: Day 40
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 4 |
Intervention Group | 3 |
The ratio between the water assimilated into the body and that lost from the body, in milliliters. (NCT04507867)
Timeframe: It is evaluated on day 3 of hospital stay (duration approximately 10 minutes).
Intervention | milliliters (Mean) |
---|---|
Control Group | 123.4 |
Intervention Group | 456.6 |
Patients who were intubated during their hospital stay and died before completing follow-up on day 40. (NCT04507867)
Timeframe: 40 days
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 5 |
Intervention Group | 1 |
The need to continue with supplemental oxygen at hospital discharge. Categories: 1. Yes, 2. No. (NCT04507867)
Timeframe: Day 40
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 23 |
Intervention Group | 26 |
Association between the presentation of certain laboratory parameters taken in the baseline period, with te overall mortality of discharge patients in comparison with deceased patients (NCT04507867)
Timeframe: Baseline
Intervention | Participants (Count of Participants) |
---|---|
Leukocytes <10x10^3/μL | 3 |
Leukocytes >10x10^3/μL | 5 |
Association between the presentation of certain laboratory parameters taken in the baseline period, with te overall mortality of discharge patients in comparison with deceased patients (NCT04507867)
Timeframe: Baseline
Intervention | Participants (Count of Participants) |
---|---|
Neutrophils <80% | 0 |
Neutrophils >80% | 8 |
Association between the presentation of certain laboratory parameters taken in the baseline period, with te overall mortality of discharge patients in comparison with deceased patients (NCT04507867)
Timeframe: Baseline
Intervention | Participants (Count of Participants) |
---|---|
RCP <150 mg/L | 1 |
RCP >150 mg/L | 7 |
Association between the presentation of certain laboratory parameters taken in the baseline period, with te overall mortality of discharge patients in comparison with deceased patients (NCT04507867)
Timeframe: Baseline
Intervention | Participants (Count of Participants) |
---|---|
Urea <40 mg/dL | 4 |
Urea >40 mg/dL | 4 |
Association between the presentation of certain laboratory parameters taken at baseline with the overall mortality of discharged patients compared to deceased patients. (NCT04507867)
Timeframe: Baseline
Intervention | Participants (Count of Participants) |
---|---|
Fibrinogen <700 mg/dL | 2 |
Fibrinogen >700 mg/dL | 6 |
Association between the presentation of certain laboratory parameters taken in the baseline period, with te overall mortality of discharge patients in comparison with deceased patients (NCT04507867)
Timeframe: Baseline
Intervention | Participants (Count of Participants) |
---|---|
Procalcitonin <0.5 ng/mL | 4 |
Procalcitonin >0.5 ng/mL | 4 |
Association between the presentation of certain laboratory parameters taken in the baseline period, with te overall mortality of discharge patients in comparison with deceased patients (NCT04507867)
Timeframe: Baseline
Intervention | Participants (Count of Participants) |
---|---|
Ureic Nitrogen <22 mg/dL | 4 |
Ureic Nitrogen >22 mg/dL | 4 |
Refers to the subjective sensation of increased abdominal pressure without an increase in abdominal size, the number of defecations were quantified at day 3 and compared between both groups. (NCT04507867)
Timeframe: Day 3
Intervention | defecations (Mean) |
---|---|
Control Group | 0.81 |
Intervention Group | 1.41 |
Is a visible increase in abdominal girth.1. Present, 2. Absent. (NCT04507867)
Timeframe: Day 3
Intervention | percent of participants (Number) |
---|---|
Control Group | 51.6 |
Intervention Group | 19.4 |
Total number of patients who died before day 40 of follow-up. (NCT04507867)
Timeframe: 40 days.
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 7 |
Intervention Group | 1 |
Overall survival, the total number of patients included in the study and completed a 40-day follow-up. (NCT04507867)
Timeframe: 40 days.
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 33 |
Intervention Group | 39 |
the total number of patients with oxygen saturation >90% on day 3 of their hospital stay. (NCT04507867)
Timeframe: day 3.
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 34 |
Intervention Group | 37 |
"The Bristol Stool Form Scale categorizes stools into one of seven stool types ranging from type 1 (hard lumps) to type 7 (watery diarrhea). Type 3 and 4 were considered Normal." (NCT04507867)
Timeframe: day 3
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 8 |
Intervention Group | 13 |
Persistence of clinical signs and symptoms that arise after developing COVID-19, and are not explained by an alternative diagnosis. 1. Present. 2. Absent. (NCT04507867)
Timeframe: Day 40.
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 9 |
Intervention Group | 8 |
total number of patients included in the study who progressed to mechanical ventilation during the first 10 days of hospital stay. (NCT04507867)
Timeframe: 10 days.
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 7 |
Intervention Group | 3 |
The oxygen saturation without supplementary oxygen is taken at the control appointment 40 days after hospital discharge. (NCT04507867)
Timeframe: day 40
Intervention | percentage (Mean) |
---|---|
Control Group | 90.39 |
Intervention Group | 92.08 |
Total number of patients who were intubated, extubated, discharged and completes the 40 day follow-up (NCT04507867)
Timeframe: 40 days
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 2 |
Intervention Group | 2 |
It is recorded for how many days the treating doctor asked the patients to continue to administer supplemental oxygen after hospital discharge (NCT04507867)
Timeframe: day 40
Intervention | days (Mean) |
---|---|
Control Group | 57.6 |
Intervention Group | 43.8 |
Is defined as at least a 5% reduction in weight from the baseline level.Total number of patients with weight loss at the end of follow-up at day 40 (NCT04507867)
Timeframe: Day 40
Intervention | Participants (Count of Participants) |
---|---|
Control Group | 8 |
Intervention Group | 8 |
Difference in oxygen delivery between the baseline period and day 3 of hospital stay in each group. (NCT04507867)
Timeframe: baseline and day 3
Intervention | Liters (L) (Mean) | |
---|---|---|
Baseline | Day 3 | |
Control Group | 5.9 | 6 |
Intervention Group | 6 | 4.5 |
Is a self-administered version of the PRIME-MD diagnostic instrument for common mental disorders, includes 9 items, which evaluate the presence of depressive symptoms based on the criteria of the Diagnostic and Statistical Manual of Mental Disorders version 4, during the last 2 weeks, how often the patient presented depressive symptoms. According to the sum of the score obtained, the following 4 categories will be considered: 0-4 minimum existence or absence of depressive symptoms; 5-9 = mild depressive symptoms; 10-14 = moderate depressive symptoms; 15-19 = moderate to severe depressive symptoms; 20-27 = severe depressive symptoms. (NCT04507867)
Timeframe: baseline and hospital discharge
Intervention | score on a scale (Mean) | |
---|---|---|
Baseline | Hospital discharge | |
Control Group | 3.66 | 1.50 |
Intervention Group | 5.3 | 1.9 |
Quick-Sequential Organ Failure Assessment (qSOFA) score gives 0 to 3 points. ≥2 in the setting of suspected infection had a high predicted in-hospital mortality rate and could be considered septic. (NCT04507867)
Timeframe: Baseline and Day 3
Intervention | score on a scale (Mean) | |
---|---|---|
Baseline | Day 3 | |
Control Group | 0.42 | 0.51 |
Intervention Group | 0.65 | 0.43 |
1 review available for clofibric acid and Osteoporosis
Article | Year |
---|---|
Lipid-lowering drugs.
Topics: Alzheimer Disease; Clofibric Acid; Diabetes Mellitus; Humans; Hydroxymethylglutaryl-CoA Reductase In | 2006 |