MedPath

Evaluation and comparison of two methods of expectant management and drug treatment with oral contraceptive pills

Phase 2
Recruiting
Conditions
Disposal of pregnancy remnants due to incomplete spontaneous abortion.
Spontaneous abortion
Registration Number
IRCT20220307054209N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
170
Inclusion Criteria

Women 15 to 45 years old
Women who had a miscarriage in the first trimester (less than 12 weeks)
Women who have had an incomplete abortion and a trans-vaginal ultrasound confirm the presence of pregnancy debris below 4 cm.
Women whose pregnancy miscarriage has been confirmed (less than 4 cm) and has been the result of a failed intrauterine pregnancy.
Patients with stable vital signs Patients asymptomatic or with spotting and mild vaginal bleeding.

Exclusion Criteria

Patients with unstable vital signs
Patients with suspected molar pregnancy
Patients with contraindications to OCP

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Disposal of pregnancy remnants due to spontaneous abortion. Timepoint: 21 days after intervention. Method of measurement: By checklist.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath