Menu
Recruiting NCT06780514

Cardiopulmonary Exercise Testing in Girls (8-18y) with Turner Sydrome.

No phase Interventional Turner Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cardiopulmonary exercise test.
Who it may be relevant to
Registry conditions: Turner Syndrome. Basic parameters: 8 years — 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Belgium
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The goal of this clinical trial is to have a beter insight in the exercise tolerance in girls with Turner Syndrome aged 8-18 years . The main question it aims to answer is: Is there a difference in VO2 max comparing Turner syndrome girls with standard values? How do cardiovascular parameters change during exercise (heart rate, bloodpressure, ...) Participants will perform a cyclo-ergometry in a standardised way.

Interventions

  • Diagnostic test Cardiopulmonary exercise test
    To our knowledge, this is the first study to perform CPET's in Turner Girls aged \<18 years

Primary outcome measures

  • VO2 max [Time frame: Whitin a week after the CPET]
Secondary outcome measures (2)
  • Bloodpressure [Time frame: Whitin a week after the CPET]
  • Heart rate [Time frame: Whitin a week after the CPET]

Eligibility criteria

Inclusion criteria

  • Turner syndrome girls aged 8-18 years old

Exclusion criteria

  • Severe mental impairement making it impossible to perform an exercise test

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

Belgium · 1 center
  • Ghent University Hospital — Ghent

Identifiers

NCT: NCT06780514 · ONZ-2023-0632

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗