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To see how drugs Atorvastatin & Atorvastatin plus Ezetimibe have effect on lipid profile in chronic kidney disease patients : A Randomised control trial

To compare the effect of Atorvastatin & Atorvastatin plus Ezetimibe on lipid profile in chronic kidney disease patients : A Randomised control trial - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054891
Enrollment
50
Registered
2023-07-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N189- Chronic kidney disease, unspecified

Interventions

Intervention1: ezetimibe plus atorvastatin: Ezetimibe- cholestrol lowering agent that inhibits absorption o cholestrol from gastroinestinal and biliary systems. Dose of Ezetimibe -10 mg/day, orally Du
HMG CoA inhibitor. Dose of Atorvastatin- 40 mg/day, orally Duration -4 weeks Control Intervention1: Atorvastatin: Atorvastatin- lipid lowering agent
HMG CoA inhibitor. Dose-40 mg/ day, orally Duration- 4weeks.

Sponsors

Dr Dolly Narwal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Who gives consent. 2. Patients with Chronic Kidney Disease between Age group of 40-60 years. 3. On Conservative Management for Chronic Kidney Disease. 4. As evidenced radiologically (Bilateral Shruken Kidney /Loss of corticomedullary differentiation) or biochemically (elevated blood urea, serum creatinine) for more than 3 months. 5. With known Chronic Kidney Disease irrespective of the etiology.

Exclusion criteria

Exclusion criteria: 1. Patients with Acute renal failure and Nephrotic syndrome. 2. Patients on drugs affecting Lipid metabolism like Beta Blockers, steroids and Oral contraceptive pills. 3. Female patients who are pregnant. 4. Known Hypothyroidism patients.

Design outcomes

Primary

MeasureTime frame
effect of drug atorvastatin and atorvastatin plus ezetimibe on lipid profile in chronic kidney disease patients.Timepoint: 4 weeks

Secondary

MeasureTime frame
To monitor the differences between the two regimens with respect to effect size profile within follow up period.Timepoint: 4 weeks

Countries

India

Contacts

Public ContactDr Dolly Narwal

MAMC AGROHA

dr.rakeshgoel16@gmail.com9215292151

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026