The effect of evening primrose in the treatment of missed abortion process.

Phase 3

Recruiting

• Conditions: Missed abortion.; Missed abortion; O02.1

• Registration Number: IRCT20160308026971N8
• Lead Sponsor: Rafsanjan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 February 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 140

Inclusion Criteria

All of women with a diagnosis of missed abortion
Inclination to participate in the study
Selection of Niknafs hospital for abortion induction

Exclusion Criteria

Vaginal bleeding
diseases associated with disorders Hemorrhagic agents, anticoagulant drugs, Patients with history of psychiatric disorders in the phenothiazine category, and epilepsy patients

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Dosage of misoprostol. Timepoint: After the abortion is complete. Method of measurement: Information recorded in the file.;Disposal time of pregnancy products. Timepoint: After the abortion is complete. Method of measurement: Information recorded in the file.;The severity of the bleeding. Timepoint: After the abortion is complete. Method of measurement: Information recorded in the file.

Secondary Outcome Measures

Name	Time	Method
Pain rate. Timepoint: During of the hospitalization. Method of measurement: Visual analogue scale.;Number of days of hospitalization. Timepoint: After the patient is discharged. Method of measurement: The information recorded in the file.;Curettage. Timepoint: During of the hospitalization. Method of measurement: The information recorded in the file.