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Clinical Trials/JPRN-UMIN000025404
JPRN-UMIN000025404Completed未知

Cervical pessary for the prevention of preterm delivery. - Preterm LabOr preVEntion, Multicenter study fOr Maternal cervical pessary(LOVE MOM)

Department of Obstetrics and Gynecology Nagoya City University, Graduate School of Medical Sciences0 sites237 target enrollmentStarted: January 15, 2017Last updated:
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Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
237
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The results of this trial suggested that cervical pessary did not reduce preterm delivery, but may delay shortening of cervical length. Vaginal discharge was increased by using cervical pessary, no other adverse events were observed. There were no cases of intrauterine fetal demise in both groups. Cervical pessary may shorten duration of hospitalization and medication. In conclusion, cervical pessary may become one of a choice of prophylactic treatment for preterm delivery.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
ot applicable to ot applicable (—)
Sex
Female

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • •1)Women with multiple pregnant. 2)Majior fetal anomalies. 3)Painful regular uterine contractions. 4)Active vaginal bleeding. 5)Placenta previa. 6)Cervical myoma. 7)History of cone biopsy or cervical cerclage in situ. 8)Other pregnant women when study doctores conclude that they are not eligible for study enrollment.

Investigators

Sponsor
Department of Obstetrics and Gynecology Nagoya City University, Graduate School of Medical Sciences

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OVE MOM trialPreterm Labor
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