Overview
Different Routes of Misoprostol Prior to First Trimester Surgical Abortion
Status:
Unknown status
Unknown status
Trial end date:
2016-07-01
2016-07-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
A randomized clinical trial to assess the effectiveness of same-day cervical preparation with oral, buccal or vaginal Misoprostol, given 2-4 hours prior first trimester curettage.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Wolfson Medical CenterTreatments:
Misoprostol
Criteria
Inclusion Criteria:- Patients admitted for elective first trimester abortion (termination of pregnancy/
missed abortion) at Wolfson Medical Center, gestational age <13+0 weeks
- Written consent supplied
Exclusion Criteria:
- Contraindications to prostaglandin treatment (severe asthma, glaucoma, severe cardiac
disease, renal failure)
- Prostaglandin allergy
- Genital infection
- Space-occupying lesion in the endocervical canal
- Prior cervical surgery