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Clinical Trials/ISRCTN44341343
ISRCTN44341343
Completed
Not Applicable

A comparison of vaginal misoprostol versus vaginal misoprostol and nitric oxide donor for termination of pregnancy at 13 to 29 weeks. A prospective randomised trial

Farhat Hached University Teaching Hospital (Tunisia)0 sites70 target enrollmentDecember 16, 2002
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Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Farhat Hached University Teaching Hospital (Tunisia)
Enrollment
70
Status
Completed
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 16, 2002
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Farhat Hached University Teaching Hospital (Tunisia)

Eligibility Criteria

Inclusion Criteria

  • •1\. All patients requiring a termination of pregnancy between 13 and 29 weeks of gestation
  • •2\. No pregnancy induced hypertension
  • •3\. No pre\-eclampsia
  • •4\. No vaginal bleeding
  • •5\. Cervix dilated less then 2 cm
  • •6\. No vaginal bleeding
  • •7\. At admission blood pressure: systolic \>120 mmHg; diastolic \>80 mmHg

Exclusion Criteria

  • •Does not match inclusion criteria

Outcomes

Primary Outcomes

Not specified

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