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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03078725
Other study ID # HSC-MS-16-1052
Secondary ID
Status Withdrawn
Phase Phase 4
First received
Last updated
Start date June 20, 2017
Est. completion date May 10, 2018

Study information

Verified date May 2018
Source The University of Texas Health Science Center, Houston
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A pragmatic, comparative effectiveness trial of glyburide versus metformin.


Description:

Patients with gestational diabetes requiring pharmaceutical treatment will be randomized to receive glyburide or metformin. Dose increases will be determined by the patient's physician. Patients will be determined to have failed either medication if glucose control can not be achieved with the maximum dose of the medication, if insulin is stared to achieve glucose control or if another oral agent is started along for glucose control.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 10, 2018
Est. primary completion date March 10, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

We will include women between 20 and 34 weeks gestational age, with a diagnosis of GDM as per the following criteria:

- 1 hour Glucose tolerance test of >130 mg/dl, followed by two abnormal values on 3 hour Glucose tolerance test, or:

- A single 1 hour Glucose tolerance test value of > 200 mg/dl, and:

- Failure to achieve glycemic control with diet and exercise or deemed to require pharmacological therapy as per physician's criteria

Exclusion Criteria:

- - Known renal impairment.

- Known hepatic disease.

- Pre-gestational diabetes.

- Known allergy to glyburide, metformin or sulfa drugs.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Glyburide
oral hypoglycemic agent
Metformin
oral hypoglycemic agent

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The University of Texas Health Science Center, Houston

Outcome

Type Measure Description Time frame Safety issue
Primary Failure rate need to start insulin therapy or another hypoglycemic agent during the pregnancy to maintain normal glucose levels or need for delivery due to hyperglycemia. from onset of oral therapy until delivery
Secondary Mean overall plasma glucose average of all postprandial glucose measurements from enrollment to delivery
Secondary Mean weekly fasting glucose average of all fasting glucose measurements from enrollment to delivery
Secondary preeclampsia preeclampsia from enrollment to delivery
Secondary cesarean section mode of delivery from enrollment to delivery
Secondary neonatal hypoglycemia neonatal hypoglycemia from enrollment to delivery
Secondary LGA infant LGA infant from enrollment to delivery
Secondary birthweight > 4500 grams birthweight > 4500 grams from enrollment to deliveryfrom enrollment to delivery
Secondary gestational age at birth gestational age at birth from enrollment to delivery
Secondary incidence of medication side effects nausea, emesis, diarrhea, abdomainal bloating from enrollment to delivery
See also
  Status Clinical Trial Phase
Terminated NCT05647798 - Intrapartum Glycemic Control in GDMA2 N/A