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Efficacy of Glibanclamide on Gestational diabetes and outcome of pregnancy

A randomized clinical trial on comparison of efficacy of Glibanclamide and insulin on Gestational Diabetes and outcome of pregnancy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016041317827N1
Enrollment
80
Registered
2016-04-13
Start date
2015-01-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Gestational Diabetes. high-risk pregnancy

Interventions

Intervention 1: Control group: Insulin will be started , if FBS or 2hpp glucose levels are not control (FBS>95/dl and 2hpp>120mg/dl) respectively by diet control and exercise. 40 patient (group A) wil
Treatment - Drugs
Control group: Insulin will be started , if FBS or 2hpp glucose levels are not control (FBS>95/dl and 2hpp>120mg/dl) respectively by diet control and exercise. 40 patient (group A) will be received In
Intervention group: 40 patients (group B) will be Glibenclamide starting with lowest requiring dose 1.25 mg (1/4 tab 5 mg) and will be increased by 1.5-2.50 mg weekly till reaching 15 mg.

Sponsors

Vice Chancellor Of Research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Maternal age 20-40 years old; singleton pregnancy; gestational age and diagnosis of gestational diabetes will be given during pregnancy; healthy mothers with no renal diseases liver diseases and overt diabetes. Exclusion criteria: If the blood glucose is not controlled by the does of 15 mg glibanclamid they will be shifted to Insulin and will be excluded the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
FBS & 2hpp. Timepoint: 4 time per day: over night fast and 2 hour post parandial diet (braekfast, lunch and dinner). Method of measurement: will be measured once a week by obestricians and twice weekly by the patients at home using Glucometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLida Tahamtani

Shiraz University of Medical Sciences

Lida.tahamtani87@gmail.com+98 71 3233 2365

Outcome results

None listed

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