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Effect of Celecxib in order to prevent spontaneous preterm labor

Phase 2
Conditions
Preterm Labor.
Preterm spontaneous labour with preterm delivery
Registration Number
IRCT2015042621947N1
Lead Sponsor
Vice-Chancellor for Research of Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
164
Inclusion Criteria

Singleton pregnancy; Intact amniotic membrane; Gestational age between 24-34 weeks; Positive tocometry. Exclusion criteria: PROM; Vaginal bleeding; Chorioamnionitis; Dilatation more than 2 cm and cervical effacement exceeding 80%; Polyhydramnios; Oligohydramnios; Intrauterine Fetal Demise; Intrauterine Growth Restriction; Fetal distress; Smoking and alcohol abuse; systemic disease; Congenital anomalies; uterine anomalies; Celecxib intolerance.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Preterm Labor. Timepoint: One hour after the onset of drug use until 24 hours. Method of measurement: Tocometer.
Secondary Outcome Measures
NameTimeMethod
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