Misoprostol for Second Trimester Termination of Pregnancy

PHASE3CompletedINTERVENTIONAL
Enrollment

130

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

December 31, 2014

Study Completion Date

December 31, 2014

Conditions
Abortion, Induced
Interventions
DRUG

Vaginal misoprostol

400 µg vaginal misoprostol per 3 hours up to 6 doses. The treatment will be withold if the patient has strong uterine contractions. If abortion had not occured in 24 hour after the start of the study a second course of 400 µg vaginal misoprostol per 3 hours up to 6 doses will be administered. If abortion had not occured in 48 hour after the start of the study it will be considered treatment failure and patient will be offered another induction/delivery method or to continue protocol.

DRUG

Buccal misoprostol

400 µg buccal misoprostol per 3 hours up to 6 doses. The treatment will be withold if the patient has strong uterine contractions. If abortion had not occured in 24 hour after the start of the study a second course of 400 µg buccal misoprostol per 3 hours up to 6 doses will be administered. If abortion had not occured in 48 hour after the start of the study it will be considered treatment failure and patient will be offered another induction/delivery method or to continue protocol.

Trial Locations (1)

25240

Ataturk Universitesi Araştırma Hastanesi, Erzurum

All Listed Sponsors
lead

Ataturk University

OTHER

NCT02048098 - Misoprostol for Second Trimester Termination of Pregnancy | Biotech Hunter | Biotech Hunter