Trial · NCT02080377
A Feasibility Study Looking at the Use of Glibenclamide and metfoRmin Versus stAndard Care in gEstational diabeteS
NCT02080377, Phase 3, Completed, University of Edinburgh
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Feasibility Study Looking at the Use of Glibenclamide and metfoRmin Versus stAndard Care in gEstational diabeteS. Trials, record NCT02080377. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02080377
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Feasibility Study Looking at the Use of Glibenclamide and metfoRmin Versus stAndard Care in gEstational diabeteS
- NCT number
- NCT02080377
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 23 participants, actual
- Lead sponsor
- University of Edinburgh
- Conditions
- Pregnancy, Gestational Diabetes
- Interventions
- Glibenclamide, Insulin
- First posted
- 2014-03-06
- Last updated
- 2016-12-08
- Other registries' IDs
- eudract:2013-004706-25
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of women willing to be randomised | 2 years | * Retention - proportion of women randomised who remain in the study to provide outcomes * Adherence - proportion of clinicians who adhere to the treatment regimen(s) |
| Secondary | Glycaemic control | 2 weekly | Safety - number of hypoglycaemic episodes needing treatment, any other adverse events |
| Secondary | Patient satisfaction | 36-38 weeks gestation | assessed by visual analogue scale |
| Secondary | Clinical outcomes | 36 weeks | Change in maternal weight between booking and 36 weeks |
| Secondary | Clinical outcome | 40 weeks | Mode and gestation of delivery. |
| Secondary | Clinical Outcome | 40 weeks | Birthweight centile (adjusted for sex and gestation at birth) |
| Secondary | Clinical Outcome | 2 days | Incidence of neonatal hypoglycaemia (defined as any of the following: blood glucose \<2.6 mmol/l) in first 48hrs age, or given intravenous glucose or any other drug to increase blood glucose) |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 28938877 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02080377
GET https://conductscience.org/api/trials/v1/NCT02080377/registered