Geneva, May 4 -- International Clinical Trials Registry received information related to the study (CTRI/2026/04/108920) titled 'Induction of labour in intrauterine fetal demise after 24 weeks of pregnancy comparing two treatment methods' on April 21.
Study Type: Interventional
Study Design:
Randomized, Parallel Group, Active Controlled Trial Method of generating randomization sequence:Computer generated randomization Method of allocation concealment:Other Blinding and masking:Outcome Assessor Blinded
Primary Sponsor: IPGMER AND SSKM HOSPITAL
Condition:
Health Condition 1: O364- Maternal care for intrauterine death
Intervention:
Intervention1: Two Dose Mifepristone Regimen: Mifepristone 200 mg orally on day 1 and day 2 followed...