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Treatment of Incomplete Abortion With 600 Mcg Oral Misoprostol Compared to Standard Surgical Treatment

NCT00674232 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 311

Last updated 2008-05-07

No results posted yet for this study

Summary

This study aims to compare the efficacy, side effects profile and acceptability of a single dose of 600mcg misoprostol taken orally compared to standard surgical treatment as per local protocols for the treatment of incomplete abortion.

Conditions

  • Incomplete Abortion

Interventions

DRUG

600 mcg misoprostol

single dose of misoprostol taken orally

PROCEDURE

Surgical treatment

Either dilation and curettage or manual vacuum aspiration, as per local protocol

Sponsors & Collaborators

  • Gynuity Health Projects

    lead OTHER

Principal Investigators

  • Melanie Peña, MPH, MA · Gynuity Health Projects

  • Jill Durocher · Gynuity Health Projects

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
14 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-05-31
Completion
2007-10-31

Countries

  • Ecuador
  • Venezuela

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00674232 on ClinicalTrials.gov