Prevention of Recurrent Preterm Delivery by a Natural Progesterone Agent

This study has been withdrawn prior to enrollment.
(Study withdrawn for financial problems. We didnwt get a grant we needed for purchesing the medication for the study.)
Information provided by:
The Baruch Padeh Medical Center, Poriya Identifier:
First received: May 23, 2006
Last updated: June 26, 2008
Last verified: June 2007
To examine the preterm delivery rate of a preterm delivery high risk group of pregnant women, using once daily natural progesterone agent.

Condition Intervention
Premature Birth
Drug: Crinone Gel 8%

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label

Resource links provided by NLM:

Further study details as provided by The Baruch Padeh Medical Center, Poriya:


Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

Pregnancy 24 weeks' gestation Preterm labor in previous pregnancies

Exclusion Criteria:

  • No medications for PTL or any kind of progesterone.
  • Cervical suture
  • Multiple pregnancy
  Contacts and Locations
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Please refer to this study by its identifier: NCT00329316

Sponsors and Collaborators
The Baruch Padeh Medical Center, Poriya
Study Chair: Yuri Perlitz, MD The Baruch Padeh Medical Center, Poriya
Principal Investigator: Mosheh Ben Ami, Prof. Head of Obs/Gyn ,The Baruch Padeh Medical center, Poriya
  More Information

No publications provided Identifier: NCT00329316     History of Changes
Other Study ID Numbers: PTL Progesterone Perlitz.CTIL 
Study First Received: May 23, 2006
Last Updated: June 26, 2008
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by The Baruch Padeh Medical Center, Poriya:
Pre-term labor

Additional relevant MeSH terms:
Premature Birth
Obstetric Labor Complications
Obstetric Labor, Premature
Pregnancy Complications processed this record on February 11, 2016