Completed

Assessment of Low Bone Mass in Premenopausal or Perimenopausal Women

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Who is being recruted

Bone Diseases+7

+ Bone Diseases, Metabolic

+ Metabolic Diseases

From 16 to 54 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: February 1998
See protocol details

Summary

Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 1998

Actual date on which the first participant was enrolled.

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.

NCT00005101
Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 16 to 54 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Bone DiseasesBone Diseases, MetabolicMetabolic DiseasesMusculoskeletal DiseasesNutritional and Metabolic DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsDisease AttributesOsteoporosisRare Diseases

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

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Columbia University College of Physicians and Surgeons

New York, United StatesOpen Columbia University College of Physicians and Surgeons in Google Maps
CompletedOne Study Center
Assessment of Low Bone Mass in Premenopausal or Perimenopausal Women | PatLynk