At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 27 enrolled
Drug / intervention
human insulin +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Safety and Efficacy of Insulin Aspart vs. Regular Human Insulin in Basal/Bolus Therapy for Patients With Gestational Diabetes
In Brief
A Phase 3 clinical trial evaluating human insulin, insulin NPH, and 1 other intervention for Diabetes and Gestational Diabetes. Completed, enrolled 27 participants across 1 site.
Detailed Summary
This trial is conducted in the United States of America (USA). The purpose of this study is to test whether NovoLog (insulin aspart) is a safe and at least as effective alternative to regular human insulin for the control of blood glucose after meals in women who develop diabetes during pregnancy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDiabetes, Gestational Diabetes
CountriesUnited States
Collaborators--
Timeline
Phase 3CompletedFinished
2000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartApr 2000
First PostedJul 2003
Primary CompletionDec 2003
TodayJul 2026
First PostedJul 18, 2003
Enrollment StartApr 1, 2000
Primary CompletionDec 1, 2003
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 23.0 years ago
Interventions
human insulindrug
insulin NPHdrug
insulin aspartdrug