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NCT06776822

The Effect of DNS Therapy on Asymmetry in Children After Surgery of Congenital Heart Disease

ENROLLING BY INVITATION NA Last updated 17 January 2025
What this trial tests

NA trial testing Dynamic neuromuscular stabilisation in Congenital Heart Disease in Children in 15 participants. Enrolling by invitation.

Timeline
20 November 2024
Primary endpoint
14 February 2025
31 May 2026

Quick facts

Lead sponsorCharles University, Czech Republic
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment15
Start date20 November 2024
Primary completion14 February 2025
Estimated completion31 May 2026
Sites1 location across Czechia

Drugs / interventions tested

Conditions studied

Sponsor

Charles University, Czech Republic

Who can join

Adults 6 to 18, any sex, with Congenital Heart Disease in Children. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This thesis will examine the consequences of congenital heart disease (CHD) surgery in children. The main goal of this work is to point out the possible development of late consequences after cardiac surgery in childhood (e.g. asymmetry, scoliosis, hypomobility of the spine) and to assess the effect of DNS therapy on the resolution of the consequences. For patients, after an intensive three-week rehabilitation intervention, an improvement in the monitored initial parameters is expected, which would lead to an improvement in the quality of life.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Congenital Heart Disease in Children

Currently open trials in the same condition.

Other Charles University, Czech Republic trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06776822.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing