Effect of Celebrex in prevention of preterm labor

Phase 2

• Conditions: O60.0, O60; Preterm labor.; Preterm labor and delivery

• Registration Number: IRCT201204232967N3
• Lead Sponsor: Vice Chancellor for research, Kashan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 200

Inclusion Criteria

pregnant women diagnosed with preterm labor pains with 4 contractions during 20 minutes or 8 contractions in an hour and having the following conditions:
1.gestational age less than 34 weeks and more than 24 weeks
2.having live singleton fetus
3.dilatation of at least 1cm
4.no exclusion criteria

Exclusion criteria: any of the following conditions:
1.ruptured amniotic membrane
2.symptoms/signs suggestive of placental detachment (decollement) 3.chorioamnionitis
4.entering the active phase of labor
5.conditions that disrupt the normal delivery process and lead to cesarean section or induction of the labor
6.no consent to participate or to continue the study by the pregnant women
7.sensitivity to the drug
8.hypertension
9.diabetes mellites
10.gastric ulcer

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
terin contractions. Timepoint: Before intervention, 1,12 and 48 hours after intervention. Method of measurement: Contractions that last more than 30 seconds and is counted by the resident during a period of 20 minutes.

Secondary Outcome Measures

Name	Time	Method
Delivery. Timepoint: 48 hours after intervention. Method of measurement: Evaluation of doing or not doing the delivery.