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NCT00240604 Clinical Trial

Prevention of Corticosteroid-induced Glucose Intolerance

Glucose Intolerance Clinical Trial

Official title:
Treatment With Rosiglitazone for the Prevention of Glucose Intolerance in Patients Treated With Corticosteroids

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00240604
Other study ID # 7-29.10.04-HMO-CTIL
Secondary ID
Status Recruiting
Phase Phase 3
First received October 16, 2005
Last updated September 13, 2011
Start date April 2005
Est. completion date October 2015

Study information
Verified date September 2011
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

Glucose intolerance is frequent and serious complication of corticosteroid therapy. the aim of the study is to examine the hypothesis that co treatment with rosiglitazone can prevent glucose intolerance in patients treated with corticosteroids.

Description:

Glucose intolerance is frequent and serious complication of corticosteroid therapy. the aim of the study is to examine the hypothesis that co treatment with rosiglitazone can prevent glucose intolerance in patients treated with corticosteroids.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date October 2015
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- corticosteroid treatment

Exclusion Criteria:

- congestive heart failure pedal edema

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Drug:
• Rosiglitazone
4 mg rosiglitazone per day

Locations
Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (1)
Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary plasma glucose concentration 6 months No
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