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Sponsored by: |
The Baruch Padeh Medical Center, Poriya |
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Information provided by: | The Baruch Padeh Medical Center, Poriya |
ClinicalTrials.gov Identifier: | NCT00329316 |
To examine the preterm delivery rate of a preterm delivery high risk group of pregnant women, using once daily natural progesterone agent.
Condition | Intervention |
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Pregnancy Premature Birth |
Drug: Crinone Gel 8% |
Study Type: | Interventional |
Study Design: | Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Pregnancy 24 weeks' gestation Preterm labor in previous pregnancies
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Exclusion Criteria:
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 |
Study ID Numbers: | PTL Progesterone Perlitz.CTIL |
Study First Received: | May 23, 2006 |
Last Updated: | June 26, 2008 |
ClinicalTrials.gov Identifier: | NCT00329316 History of Changes |
Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
Pre-term labor progesterone |
Pregnancy Complications Progesterone Hormone Antagonists Progestins Obstetric Labor, Premature |
Hormones, Hormone Substitutes, and Hormone Antagonists Obstetric Labor Complications Hormones Recurrence Premature Birth |
Pregnancy Complications Progesterone Progestins Obstetric Labor, Premature Physiological Effects of Drugs |
Hormones, Hormone Substitutes, and Hormone Antagonists Obstetric Labor Complications Hormones Pharmacologic Actions Premature Birth |