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Clinical Trials/TCTR20140427001
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.

Registry
who.int
Start Date
April 27, 2014
End Date
March 30, 2014
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Faculty of medicine, Thammasat University

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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