ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Study of Low Bone Mass in Premenopausal or Perimenopausal Women

This study has been completed.

Sponsors and Collaborators: National Center for Research Resources (NCRR)
Columbia University
Information provided by: National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier: NCT00005101
  Purpose

OBJECTIVES:

I. Determine the possible causes of bone loss in premenopausal or perimenopausal women.


Condition
Osteoporosis

MedlinePlus related topics:   Osteoporosis   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Screening

Further study details as provided by National Center for Research Resources (NCRR):

Study Start Date:   February 1998

Detailed Description:

PROTOCOL OUTLINE: Patients undergo physical examination and complete history with emphasis on risk factors for osteoporosis and screening for occult secondary causes of osteoporosis through blood serum and 24 hour urine collection.

Patients with more than 6 months since prior bone mineral density measurements or who did not receive measurements at participating center, undergo dual energy x-ray absorptiometry over 30 minutes for bone mineral density measurements.

  Eligibility
Ages Eligible for Study:   16 Years to 54 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

  • Low bone mass (T score less than -2.0) with no secondary cause on routine exam
  • Premenopausal

OR

  • Perimenopausal

--Prior/Concurrent Therapy--

  • Chemotherapy: No prior or concurrent chemotherapeutic agents
  • Endocrine therapy: No prior or concurrent glucocorticoids or suppressive doses of thyroid hormone
  • Other: No prior or concurrent anticonvulsants

--Patient Characteristics--

  • Hematopoietic: No multiple myeloma
  • Other: No hyperparathyroidism No thyrotoxicosis No anorexia nervosa No Paget's disease of bone No rheumatoid arthritis No Cushing's syndrome No malabsorption syndrome No type I diabetes mellitus
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00005101

Locations
United States, New York
Columbia University College of Physicians and Surgeons    
      New York, New York, United States, 10032

Sponsors and Collaborators

Investigators
Study Chair:     Elizabeth Shane     Columbia University    
  More Information


Study ID Numbers:   NCRR-M01RR00645-2738, CPMC-IRB-8414, CPMC-GCRC-2738
First Received:   April 6, 2000
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00005101
Health Authority:   United States: Federal Government

Keywords provided by National Center for Research Resources (NCRR):
disease-related problem/condition  
osteoporosis  
rare disease  

Study placed in the following topic categories:
Musculoskeletal Diseases
Rare Diseases
Osteoporosis
Bone Diseases, Metabolic
Bone Diseases

ClinicalTrials.gov processed this record on December 03, 2008




Links to all studies - primarily for crawlers