TCTR20140427001
Completed
Phase 3
The Effectiveness of Sublingual or Oral Administration Misoprostol for Cervical Ripening before Manual Vacuum Aspiration in First Trimester Termination of Pregnancy: Randomized Controlled Trial
Faculty of medicine, Thammasat University0 sites80 target enrollmentApril 27, 2014
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- First trimester termination of pregnancyThe effectiveness of Misoprostol for cervical preparation before manual vacuum aspiration
- Sponsor
- Faculty of medicine, Thammasat University
- Enrollment
- 80
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •A singleton intrauterine pregnancy equal or less than 12 weeks gestational age with a diagnosis of early pregnancy failure blighted ovum anembryonic gestation and embryonic death no cardiac activity visible on TVS when the embryo measures 5 mm or more in length The gestational age was verified by a reliable menstrual history and confirmed by physical or ultrasound examination
Exclusion Criteria
- •A history of misoprostol allergy
- •anticoagulant usage
- •clinical coagulopathy
- •bleeding disorder
- •hypertension
- •chronic illness
- •active pelvic inflammatory disease
- •inevitable and incomplete abortion
Outcomes
Primary Outcomes
Not specified
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