CTRI/2018/11/016452CompletedPhase 4
An observational analysis of effect of rosuvastatin vs atorvastatin on glucose metabolism and cognitive function in dyslipidemic patients in medicine department S.N.M.C Agra.
il0 sites118 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Enrollment
- 118
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
Inclusion Criteria
- •diagnosed cases of dyslipidemia on atorvastatin or rosuvastatin therapy in all doses prescribed by the clinician
Exclusion Criteria
- •patients in whom an additional statin therapy could be detrimental or additive for adverse effects like myopathy and raised liver enzymes were excluded. such categories include:-
- •Patients with h/o liver disease or hepatic failure.
- •Pregnant and lactating women.
- •Patients with h/o serious or hypersensitivity reactions to statins.
- •Patients with documented h/o coronary artery disease or other atherosclerotic disease.
- •Patients of familial hypercholesterolemia.
- •Patients taking other class of hypolipidemic drugs (fibrates, niacin) and taking other cardiac drugs like Verapamil and Amiodarone
- •Patients taking Immunosupressants, Azole antifungal agents, Protease inhibitors.
Investigators
Similar Trials
Not yet recruiting
Not Applicable
An Observational clinical study to find out co-relation between Rasadushti in Sthaulya (Obese) Patients with HypothyroidismCTRI/2019/12/022409isha Tripathi
Recruiting
Not Applicable
Prospective observational study of the effect of romosozumab in postmenopausal osteoporotic women with inadequate response to existing osteoporosis treatmentOsteoporosis, PostmenopausalD015663OsteoporosisJPRN-jRCT1051210070Yamamoto Misa20
Not yet recruiting
Unknown
Effects of Rajo Sevan on Udan Vayu Karma: A Study in Stone Crusher Workers.CTRI/2024/02/062986Dr. Nikita Sitaram Shelke
Recruiting
Not Applicable
A Two-Part Study to Assess the Effects of Ritonavir on PRN1008 Pharmacokinetics, and the Effect of PRN1008 on QTc Interval Compared to Placebo and Moxifloxacin in Healthy ParticipantsPemphigusImmune Thrombocytopenic PurpuraACTRN12618001036202Principia Biopharma, Inc.40
Completed
Not Applicable
A study of the efficacy of the addition of a ropivacaine infusion to the analgesia provided by pre-emptive ropivacaine and intra-operative parecoxib for peri-operative pain management in adults undergoing elective arthroscopic rotator cuff surgery: a randomised double blind placebo controlled trial.Rotator cuff surgeryMusculoskeletal - Other surgeryACTRN12606000195550Monash University, Jennifer Coghlan PhD Scholar, Supervisors, A/Prof. Rachelle Buchbinder and A/Prof. Andrew Forbes.158