NCT00433303

Brief Summary

The purpose of our study is correlate between premature delivery (between week 23-35 of the pregnancy) in women that had intercourse up to 12 hours prior to beginning of labor and polymorphisms in the gene Prostanoid receptor.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 8, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 9, 2007

Completed
Last Updated

February 9, 2007

Status Verified

February 1, 2007

First QC Date

February 8, 2007

Last Update Submit

February 8, 2007

Conditions

Labor OnsetGravidity

Interventions

Correlation between early delivery and coital activityBEHAVIORAL

Eligibility Criteria

Age20 Years - 40 Years
Sexfemale
Age GroupsAdult (18-64)

You may qualify if:

  • Women who start delivery in weeks 23-35 of pregnancy 12 hours after intercourese.
  • Women who come for delivery after week 31 and have not had intercourse during the previous month.
  • Women at term who have been sexually active during their pregnancy.

You may not qualify if:

  • Any other women who come in for delivery.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shaare Zedek Medical Center

Jerusalem, 91031, Israel

Location

Related Publications (1)

  • Brustman LE, Raptoulis M, Langer O, Anyaegbunam A, Merkatz IR. Changes in the pattern of uterine contractility in relationship to coitus during pregnancies at low and high risk for preterm labor. Obstet Gynecol. 1989 Feb;73(2):166-8.

    PMID: 2911421BACKGROUND

Study Officials

  • Michael Schimmel, Prof.

    Neonatology Unit, Shaare Zedek Medical Center, Jerusalem, Israel

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Michael Schimmel, Prof.

CONTACT

972-2-6550689schimmel@New.szmc.org.il

Study Design

Study Type
observational
Observational Model
DEFINED POPULATION
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

February 8, 2007

First Posted

February 9, 2007

Last Updated

February 9, 2007

Record last verified: 2007-02

Locations

IL(1)