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Transient Osteoporosis of Pregnancy: A Possible Peptide Mediator

This study has suspended participant recruitment.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00541645
First Posted: October 10, 2007
Last Update Posted: March 18, 2008
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.
Information provided by:
Hadassah Medical Organization
  Purpose

Transient osteoporosis of pregnancy (TOoP) is uncommonly encountered in orthopedic and obstetric practice, with most reports consisting of single cases.

This rare condition consists of significant osteoporosis affecting the hips and spine, causing significant morbidity, and putting young female patients at risk for vertebral and femoral neck fractures.

The pathogenesis of transient osteoporosis of pregnancy is unknown, with various theories as to its etiology.

Recently, a number of reports have described elevated levels of PTHrP in patients with transient osteoporosis in pregnancy and of the postpartum period Our goal in this study is to assess the role of PTHrP in transient osteoporosis of pregnancy


Condition
Transient Osteperosis

Study Type: Observational
Study Design: Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Criteria

Inclusion Criteria:

  • Signed Informed consent
  Contacts and Locations
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 ClinicalTrials.gov identifier (NCT number): NCT00541645


Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Efrain Liebner, MD Hadassah Medical Organization
Study Chair: Meir Liebergall, M.D Hadassah Medical Organization
Study Director: Tzvi Bar-Shavit, Ph.D The Hebrew University
  More Information

ClinicalTrials.gov Identifier: NCT00541645     History of Changes
Other Study ID Numbers: Lib001-HMO-CTIL
First Submitted: October 7, 2007
First Posted: October 10, 2007
Last Update Posted: March 18, 2008
Last Verified: March 2008