ClinicalTrials.Veeva

Menu

Long Term Follow-up of Bone Mineral Density in Hormone Treated Turner Syndrome

University of Aarhus logo

University of Aarhus

Status

Unknown

Conditions

Turner Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT00625001
1994/2424

Details and patient eligibility

About

Turner Syndrome (TS) is associated with osteopenia and osteoporosis. Reduced bone mineral density (BMD) and increased risk of fractures are present in many younger and middle-aged women with TS. The objective is therefore to describe longitudinal changes in BMD in TS.

The study is an observational follow-up study. Examinations at baseline, after 5 and 10 years.

Bone mineral density is measured by dual energy x-ray absorptiometry (DEXA) and bone turnover by bone markers.

Main Outcome Measures: Bone mineral density (BMD; grams/ square centimetre) were measured at lumbar spine, hip and the non-dominant forearm.

Enrollment

54 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Turner syndrome verified by karyotyping

Exclusion criteria

  • untreated hypothyroidism or hyperthyroidism
  • present or past malignant diseases
  • clinical liver disease
  • treatment with drugs known to interfere with bone metabolism (e.g. glucocorticoids)

Trial design

54 participants in 2 patient groups

1
Description:
Women with Turner syndrome
2
Description:
Healthy control women

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems