Geneva, March 23 -- International Clinical Trials Registry received information related to the study (ISRCTN71047458) titled 'A study to investigate a tailor-made device designed to insert an intrauterine contraceptive device (IUD) immediately after childbirth' on March 10.
Study Type: Interventional
Study Design:
Allocation: Randomized controlled trial
Masking: Blinded (masking used)
Control: Active
Assignment: Single
Purpose: Device feasibility
Primary Sponsor: Accord (United Kingdom)
Condition:
Contraception
Pregnancy and Childbirth
Intervention:
The device under investigation is a postpartum IUD (PPIUD), which consists of a dedicated postpartum inserter and a pre-loaded (copper) CU-IUD. The postpartum inserter is a long tube ...