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| Sponsor: | The Baruch Padeh Medical Center, Poriya |
|---|---|
| Information provided by: | The Baruch Padeh Medical Center, Poriya |
| ClinicalTrials.gov Identifier: | NCT00329316 |
Purpose
To examine the preterm delivery rate of a preterm delivery high risk group of pregnant women, using once daily natural progesterone agent.
| Condition | Intervention |
|---|---|
|
Pregnancy Premature Birth |
Drug: Crinone Gel 8% |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label |
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Pregnancy 24 weeks' gestation Preterm labor in previous pregnancies
-
Exclusion Criteria:
Contacts and Locations| 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
| ClinicalTrials.gov 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 |
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Pre-term labor progesterone |
|
Premature Birth Obstetric Labor, Premature Obstetric Labor Complications Pregnancy Complications Progestins |
Progesterone Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Pharmacologic Actions |