NCT00329316

Brief Summary

To examine the preterm delivery rate of a preterm delivery high risk group of pregnant women, using once daily natural progesterone agent.

Trial Health

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 23, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

May 24, 2006

Completed
Last Updated

June 27, 2008

Status Verified

June 1, 2007

First QC Date

May 23, 2006

Last Update Submit

June 26, 2008

Conditions

PregnancyPremature Birth

Keywords

Pre-term laborprogesterone

Interventions

Crinone Gel 8%DRUG

Eligibility Criteria

Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Pregnancy 24 weeks' gestation Preterm labor in previous pregnancies

You may not qualify if:

  • No medications for PTL or any kind of progesterone.
  • Cervical suture
  • Multiple pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Premature Birth

Condition Hierarchy (Ancestors)

Obstetric Labor, PrematureObstetric Labor ComplicationsPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital Diseases

Study Officials

  • Yuri Perlitz, MD

    The Baruch Padeh Medical Center, Poriya

    STUDY CHAIR

  • Mosheh Ben Ami, Prof.

    Head of Obs/Gyn ,The Baruch Padeh Medical center, Poriya

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

May 23, 2006

First Posted

May 24, 2006

Last Updated

June 27, 2008

Record last verified: 2007-06