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Clinical Trial Summary

A randomize trial: expectation or evacuatio uteri for the treatment after late abortion


Clinical Trial Description

A randomize trial adressing 200 women consecutively recruited from clinical practice at Rigshospitalet.Expectation: administration of 800 microgram Cytotec half an hour after delivery. Surgery: Evacuation of the uterus ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00256009
Study type Interventional
Source Rigshospitalet, Denmark
Contact Lars Alling Møller, Md phd
Phone 0045 35451338
Email Lars.Alling@rh.dk
Status Not yet recruiting
Phase Phase 4
Completion date January 2009

See also
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Recruiting NCT02480543 - Different Routes of Misoprostol Prior to First Trimester Surgical Abortion Phase 4
Completed NCT00870272 - Study of 400mcg Sublingual Versus 400mcg Buccal Misoprostol Following 200mg Mifepristone for Medical Abortion up to 63 Days Last Menstrual Period (LMP) N/A
Completed NCT02048098 - Misoprostol for Second Trimester Termination of Pregnancy Phase 3