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The Effect of Laminaria with Vaginal Misoprostol on Cervical Preparation in Induction of Second Trimester Abortio

Phase 3
Recruiting
Conditions
Medical abortion.
Complications following (induced) termination of pregnancy
Registration Number
IRCT20190529043759N1
Lead Sponsor
Zahedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
90
Inclusion Criteria

Pregnant women between 14-20 weeks of pregnancy at Imam Ali Hospital who are candidates for termination of pregnancy
due to severe anomalies
or due to fetal death
Singleton conditions, parity 1 to 3, painless and uterine infections

Exclusion Criteria

Allergy to the drug
parity of more than three
severe anemia
active liver disease
cardiovascular disease
uncontrolled seizures
having IUD
Placenta Previa
History of cesarean section
previous incision on the uterus
Use of corticosteroids
Use of anti coagulants

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Termination of pregnancy. Timepoint: Every eight hours to six times. Method of measurement: dilatation of cervix and contraction.
Secondary Outcome Measures
NameTimeMethod
eed for curettage. Timepoint: From the start, every eight hours to six turns. Method of measurement: Clinical examinations.;Abortion time in labor. Timepoint: Interval between administration of drug and expulsion of fetus. Method of measurement: Record time.;Time of admission in hospital after abortion. Timepoint: From the time of the abortion to the patient's discharge. Method of measurement: Record time.
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