Working… Menu
Trial record 78 of 143 for:    NIFEDIPINE

Bryophyllum vs. Nifedipine

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00391339
Recruitment Status : Unknown
Verified October 2006 by Weleda AG.
Recruitment status was:  Not yet recruiting
First Posted : October 23, 2006
Last Update Posted : October 23, 2006
Information provided by:
Weleda AG

Brief Summary:
In a prospective, randomised study the efficacy and tolerability of bryophyllum p. (p.o) vs. nifedipine (p.o) will be proofed in a defined group of pregnant women with threatened preterm labour.

Condition or disease Intervention/treatment Phase
Tocolysis Drug: Bryophyllum p. Phase 2 Phase 3

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Enrollment : 140 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Bryophyllum p. Versus Nifedipine for the Treatment of Premature Contractions
Study Start Date : November 2006
Study Completion Date : October 2008

Resource links provided by the National Library of Medicine

Drug Information available for: Nifedipine

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Female

Exclusion Criteria:

  • Bishop Score > 5

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00391339

Layout table for location information
Department of Obstetrics, University of Zuerich Not yet recruiting
Zuerich, Switzerland, 8091
Principal Investigator: Roland Zimmermann, Prof. Dr. med.         
Principal Investigator: Ursula von Mandach, Prof. Dr. pharm.         
Sponsors and Collaborators
Weleda AG
Layout table for investigator information
Principal Investigator: Roland Zimmermann, Prof. Dr. med. Department of Obstetrics, University Zuerich

Layout table for additonal information Identifier: NCT00391339     History of Changes
Other Study ID Numbers: CI-C-64-Wel-06
First Posted: October 23, 2006    Key Record Dates
Last Update Posted: October 23, 2006
Last Verified: October 2006
Keywords provided by Weleda AG:
Bryophyllum p.
Additional relevant MeSH terms:
Layout table for MeSH terms
Calcium Channel Blockers
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Calcium-Regulating Hormones and Agents
Physiological Effects of Drugs
Vasodilator Agents
Tocolytic Agents
Reproductive Control Agents