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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01734486
Other study ID # GHTUR/F/3
Secondary ID
Status Completed
Phase Phase 4
First received November 22, 2012
Last updated February 27, 2017
Start date September 23, 1996
Est. completion date May 21, 2003

Study information

Verified date February 2017
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial is conducted in Europe. The aim of the trial is to evaluate growth response of two somatropin dose regimens in girls with Turner Syndrome.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date May 21, 2003
Est. primary completion date May 21, 2003
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Turner syndrome

- If age below 3 years, either body height below - 1 SD (standard deviation) with average growth velocity according to chronological age or body height below 0 SD with growth velocity below -1 SD according to chronological age

- If age above 3 years, body height below - 1 SD with average growth velocity according to chronological age

- Measured parental height available

- Written informed consent

Study Design


Intervention

Drug:
somatropin
0.9 UI/kg/week. Subcutaneous injection for 3 years
somatropin
1.8 UI/kg/week. Subcutaneous injection for 3 years

Locations

Country Name City State
France Novo Nordisk Investigational Site Besancon
France Novo Nordisk Investigational Site Bordeaux
France Novo Nordisk Investigational Site Dunkerque
France Novo Nordisk Investigational Site Grenoble
France Novo Nordisk Investigational Site Lille
France Novo Nordisk Investigational Site Lorient
France Novo Nordisk Investigational Site NICE cedex 3
France Novo Nordisk Investigational Site Paris
France Novo Nordisk Investigational Site Reims
France Novo Nordisk Investigational Site Rennes
France Novo Nordisk Investigational Site Rouen
France Novo Nordisk Investigational Site Tarbes
France Novo Nordisk Investigational Site TOULOUSE cedex
France Novo Nordisk Investigational Site Tours
France Novo Nordisk Investigational Site Vandoeuvre Les Nancy

Sponsors (1)

Lead Sponsor Collaborator
Novo Nordisk A/S

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Height gain, SDS (Standard Deviation Score)
Primary Height gain in cm
Secondary Height
Secondary Bone maturation
See also
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Completed NCT00471731 - Dry Eye in Women With Turner Syndrome and Women With Premature Ovarian Failure N/A
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Completed NCT03181230 - Health, Fitness, and Quality of Life in Adolescent Girls With Turner Syndrome
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