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Comparison of Effect of Bromocriptine mesylate and Pioglitazone in uncontrolled type 2 Diabetic Patients

Comparison of Efficacy of Bromocriptine mesylate and Pioglitazone in Type 2 Diabetes Patients: A Randomized open labeled Controlled clinical trial. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/12/002306
Enrollment
60
Registered
2011-12-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: E119- Type 2 diabetes mellitus without complications Health Condition 2: null- Uncontrolled Type 2 Diabetes

Interventions

Intervention1: Tab Bromocriptine mesylate 0.8 mg quick release formulaton: Bromociptine tablet 0.8 mg (1 tablet) daily will be given in first week, followed by 1.6 mg (2 tablets) in 2nd week, later 2.

Sponsors

Smt Kashibai Navale Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between 30 to 70 years Sex: Male or Non-lactating female HbA1 more than 8 Type 2 Diabetic patient on Sulphonylureas or Metformin not responding adequately

Exclusion criteria

Exclusion criteria: Age less than 30 yrs. Pregnancy Lactating mother Patient with Insulin dependent Diabetes Mellites Patient who is taking oral antidiabetic drugs other than Sulphonyureas and Metformin Severe and Complicated diabetes Patient with IHD Patients having renal or hepatic dysfunction Patient of Parkinsonism, syncopal migraine Patient who is taking Salicylates, Sulfonamides, Chloramphenicol, Probenecid, Phenithiazines, Butyrophenones, Thioxanthenes,Metoclopramide Strong Inhibitors/Inducers/ Substrates of CYP 3A4 Inhibitors -sodium valproate, erythromycin, Fluroquinolones except ofloxacin, verapamil, diltiazem, propoxyphene, allopurinol, MAO inhibitors, disulfiram, tolbutamide, metronidazole,captopril, enalpril, carbidopa Inducers :Phenobarbitone, phenytoin, carbamazepine, ethanol, clofibrate, griseofulvin, Rifampcin, pyridoxine Substrates: barbiturates, warfarin,theophylline, paracetamol, ascorbic acid, dextropropoxyphene, tolbutamide, diazepam, vit D, oral contraceptives, antidepressants, quinidine, terfanidine,phenytion, carbamazepine, morphine, pethidine, HIV positive patients

Design outcomes

Primary

MeasureTime frame
To compare glycemic control measured by fasting and postmeal levels of HbA1c between Bromocriptine and Pioglitazone To compare fasting and postmeal blood sugar level between Bromocriptine and Pioglitazone Fasting and postmeal serum insulin level between Bromocriptine and Pioglitazone To comapre adverse effects between Bromocriptine and Pioglitazone Timepoint: baseline 1 2 3 6 months

Secondary

MeasureTime frame
To compare Serum LDL, HDL, VLDL, Triglycerides, Total Cholesterol between Bromocriptine and Pioglitazone To compare blood pressure between Bromocriptine and Pioglitazone To compare weight reduction between Bromocriptine and Pioglitazone Timepoint: baseline 1 2 3 6 months

Countries

India

Contacts

Public ContactDr Yogendra N Keche

Smt Kashibai Navale Medical College and Hospital

drynkeche@gmail.com02024106148

Outcome results

None listed

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