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Clinical Trials/IRCT20180821040844N1
IRCT20180821040844N1
Completed
Phase 3

Effect of a Single Preoperative Dose of Sublingual Misoprostol on Intraoperative Blood Loss During Total Abdominal Hysterectomy

Iran University of Medical Sciences0 sites132 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Iran University of Medical Sciences
Enrollment
132
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patient who were Nominated for Abdominal Hysterectomy due to Benign Gynecologic Disease

Exclusion Criteria

  • Misoprostol Contraindication
  • Malignant Gynecologic Disease

Outcomes

Primary Outcomes

Not specified

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