Skip to content

To study levels of calcium, phosphorous and vitamin in body fluids before and after a 12 weeks course of pioglitazone, an anti diabetic agent, in pateints with diabetes

EFFECT OF PIOGLITAZONE ON RENAL CALCIUM AND PHOSPHATE HANDLING AND SERUM VITAMIN D OF PATIENTS WITH DIABETES - POCPDD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/04/002597
Enrollment
30
Registered
2012-04-24
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: null- type 2 diabetes

Interventions

Intervention1: Pioglitazone: 45 mg/day of pioglitazone orally after food in three divided doses for 12 weeks

Sponsors

RSSDI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients attending diabetic clinic or endocrine out patient department (OPD) services of SSKM Hospital and IPGMER will be considered. Patients of type 2 diabetes not controlled (fasting sugar >110, Post prandial > 180 or HbA1C >6.5) on medical nutrition therapy and metformin would be undertaken for the study

Exclusion criteria

Exclusion criteria: 1)Patients with very poorly controlled sugars i.e. HbA1C more than 8 will not be enrolled since glycosuria is associated with hypercaiciuria and control of glycemic status with pioglitazone can decrease calcium excretion and confound results 2)Patients taking insulin and/or other anti-diabetic drugs will be excluded. Patients on ACE inhibitors and diuretics will be excluded as will patients having blood pressures above 180systolic or diastolic above 110 mm Hg 3)Also patients with associated disorders like primary hyperparathyroidism, chronic kidney disease, liver disease, any chronic illness, malignancy, chronic drug use like anti-epileptic agents, oral contraceptive pills, steroids which are likely to interfere with vitamin-D metabolism will be excluded. 4)Patients with pregnancy would be excluded. Patients on calcium or vitamin-D supplementation would also be excluded.

Design outcomes

Primary

MeasureTime frame
1) effect on urinary calcium and phosphate excretion 2) effect on serum vitamin D and 1,25 vitamin D levelsTimepoint: 1) effect on urinary calcium and phosphate excretion 2) effect on serum vitamin D and 1,25 vitamin D levels

Secondary

MeasureTime frame
effect on glycemic controlTimepoint: 3 months

Countries

India

Contacts

Public ContactAnubhav Thukral

Professor, Dept of Endocrinology & Metabolism (THESIS GUIDE)

satinath.mukhopadhyay@gmail.com09830027985

Outcome results

None listed

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