NCT06641141 The Feasibility Of Expectant Management Versus Induction At 38 Weeks Among Individuals With Gestational Diabetes Mellitus: A Randomized Controlled Pilot Trial (EAGER Pilot Trial)
| NCT ID | NCT06641141 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ottawa Hospital Research Institute |
| Condition | Gestational Diabetes Mellitus (GDM) |
| Study Type | INTERVENTIONAL |
| Enrollment | 260 participants |
| Start Date | 2025-04-07 |
| Primary Completion | 2027-09 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 260 participants in total. It began in 2025-04-07 with a primary completion date of 2027-09.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The EAGER pilot trial is designed to assess the feasibility of a Canadian, multicentre prospective randomized open-label blinded end-point (PROBE) clinical trial addressing whether induction of labour (IOL) at 38 weeks' gestation compared to expectant management (EM) reduces severe perinatal mortality and morbidity among individuals with gestational diabetes mellitus (GDM). Eligible participants will be consented between 32 weeks + 0 days and 38 weeks + 0 days gestation and randomized between 36 weeks + 0 days and 38 weeks + 0 days gestation. Participants will be randomized to one of two arms: * Intervention Arm: IOL between 38 weeks + 0 days and 38 weeks + 6 days OR * Control Arm: EM without intervention until spontaneous labour, or earlier if a medical indication arises. A total of 260 participants (130 per group) will be recruited from Canadian sites, where participants will have 3 study visits: 1. Enrollment and randomization 2. After delivery and up to 72 hours postpartum 3. 6 weeks postpartum At enrollment and randomization, patient-reported baseline and clinical data from medical charts will be collected. Upon admission to hospital for labour and delivery, a blood sample may be collected to assess HbA1C and plasma glucose levels. After delivery and up to 72 hours postpartum, study feasibility will be assessed through patient-reported outcomes and administrative and clinical data. At 6 weeks postpartum, participants will be surveyed for secondary health resource use. Findings from this pilot will inform the design, implementation and feasibility of a future full-scale randomized controlled trial.
Eligibility Criteria
Inclusion Criteria: * Diagnosis of GDM after 24 weeks of gestation, based on documented 1-step or 2-step screening and diagnostic tests for GDM. * Singleton fetus at randomization. * Confirmed live fetus within 24 hours prior to randomization. * Gestational age between 36 weeks + 0 days and 38 weeks + 0 days inclusive based on an ultrasound in the first or second trimester \[≤ 23 weeks + 0 days\]. For pregnancies conceived by in vitro fertilization, dating will be based on the embryo age at transfer. * Cephalic presentation. * Planning to deliver at a participating site. * Aged 16 years or older. Exclusion Criteria: * Pre-pregnancy diabetes mellitus. * Any obstetrical/maternal indication for immediate delivery including placenta abruption, abnormal fetal well-being either by non-stress test or biophysical profile, history of venous thromboembolism (VTE) on low molecular weight heparin, pre-existing hypertension, gestational hypertension, preeclampsia, eclampsia, or Hemolysis, elevated liver enzymes and low platelets (HELLP) syndrome at the time of randomization. * Contraindication to labour and/or vaginal delivery. * Signs of labour (regular uterine contractions accompanied by cervical dilation and/or effacement) at the time of randomization. * Significant vaginal bleeding or ruptured membranes at the time of randomization. * Prior Cesarean delivery. * Placenta previa, placenta accreta, or vasa previa. * Cerclage in current pregnancy. * Known major fetal anomaly (e.g., gastroschisis, congenital heart defects). * Known oligohydramnios (AFI \< 5 or MVP \< 2 or no 2 by 2 pocket). * Known fetal growth restriction (EFW \< 3rd percentile). * Refusal of blood products. * Use of unregulated substances.
Contact & Investigator
Mark C Walker, MD, MSc, MHM
PRINCIPAL INVESTIGATOR
Ottawa Hospital Research Institute
Frequently Asked Questions
Who can join the NCT06641141 clinical trial?
This trial is open to female participants only, aged 16 Years or older, studying Gestational Diabetes Mellitus (GDM). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06641141 currently recruiting?
Yes, NCT06641141 is actively recruiting participants. Contact the research team at malmurphy@ohri.ca for enrollment information.
Where is the NCT06641141 trial being conducted?
This trial is being conducted at Ottawa, Canada.
Who is sponsoring the NCT06641141 clinical trial?
NCT06641141 is sponsored by Ottawa Hospital Research Institute. The principal investigator is Mark C Walker, MD, MSc, MHM at Ottawa Hospital Research Institute. The trial plans to enroll 260 participants.
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