Clinical Trials Directory

Trials / Completed

CompletedNCT00134745

Defining the Optimal Hormonal Replacement Therapy in Turner Syndrome

The Growth of Genitalia Interna and the Bone Mineralization Under Hormonal Replacement Therapy and the Presence of Aortic Root Dilatation in Girls With Turner Syndrome

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
43 (actual)
Sponsor
Line Cleemann · Academic / Other
Sex
Female
Age
10 Years – 25 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to examine whether a larger dosage of estrogen than the one used today will secure the development of a normal sized uterus and increase the strength of the bones in girls and young women with Turner syndrome. The purpose is also to evaluate whether aortic dilatation is present in this group of patients, and if the estrogen dosage will influence the emotional well-being and self-esteem of the patients.

Detailed description

Turner syndrome is a common chromosomal disorder with only one X-chromosome or partial deletions in one X-chromosome in all or some of the cell-lines in the body. Appr. 18 girls/year are being born with the syndrome in Denmark. The syndrome is mostly known for reduced final height and the lack of pubertal development with infertility, but it is also known for diseases influencing other parts of the body like the heart with the risk of development of aortic dilatation and subsequently dissection with the risk of rupture, profuse bleeding and sudden death. Reduced bone strength and increased risk of bone fracture are also features of the syndrome. Treatment with growth hormone and female sex-hormones are well-established treatments. Girls and young women with Turner syndrome ages 10 to 21 years will participate. The girls ages 15 to 21 years will randomly and double blindly receive treatment with either 2 mg or 4 mg estrogen for 5 years. Yearly examinations with blood tests, physical examinations, questionnaires, ultrasound and MR-scan of the internal female genitalia, DEXA-scan of the bones and MR-scan of the heart will be performed.

Conditions

Interventions

TypeNameDescription
DRUGestradioltablets, 2 mg day 1 through day 22 of the menstrual cycle for 5 years

Timeline

Start date
2005-06-01
Primary completion
2013-03-01
Completion
2013-03-01
First posted
2005-08-25
Last updated
2013-06-14

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00134745. Inclusion in this directory is not an endorsement.