Remote Assesment of Functional Sequelae in Patients Operated for Congenital Syndactyly
DISTSSEQUELO
Evaluation of the Gilbert Dorsal Commissural Flap in the Managment of Congenital Syndactylies
2 other identifiers
observational
37
1 country
1
Brief Summary
The aim of th study is to evaluate patients who have been operated for congenital syndactylies. The surgical technique has evolved, and the donnor site for the total skin graft is not the same than 10 years ago. Furthermore, the investigators want to evaluate the function of the hand and the evolution of the operated web space. The patient is examined in consultation by the same doctor, the investigator list complications and evolution of the hand. the investigators also ask the patient and his parents about the satisfaction of the surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Dec 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 13, 2023
CompletedStudy Start
First participant enrolled
December 7, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedFirst Posted
Study publicly available on registry
May 19, 2026
CompletedMay 19, 2026
May 1, 2026
12 months
November 13, 2023
May 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Study of the retraction of the webspace with Withey scale
From 4 years to 18 years after the surgery
Secondary Outcomes (1)
Evaluation of the scars with Vancouver scale.
From 4 years to 18 years after the surgery
Other Outcomes (4)
Evaluation of the scar from the donor site of the total skin graft with Vancouver scale.
4 years to 18 years after the surgery
Study of the flessum with a goniometer.
4 years to 18 years after the surgery
Study of the clinodactyly with a goniometer.
4 years to 18 years after the surgery
- +1 more other outcomes
Study Arms (1)
Consultation
Patients will be called in for consultation in the CHU de Lille to be examined.
Interventions
Patients will be called in for consultation in the CHU de Lille to be examined.
Eligibility Criteria
Il s'agit d'une cohorte de patients opérés d'une syndactylie congénitale des doigts longs. On étudie ici la rétraction commissurale et les séquelles fonctionnelles et esthétiques, avec greffe de peau totale prélevée au niveau du pli du poignet.
You may qualify if:
- operated between 2005 and 2019 at Lille University Hospital.
- born between 2003 and 2020.
- With congenital syndactyly (ies) of the upper limb.
- Syndromic or non syndromic congenital syndactyly of the upper of the long fingers.
You may not qualify if:
- Patients operated on before 2005 or after 2020
- Acquired syndactyly (post-traumatic)
- Syndactyly (ies) of the lower limb.
- congenital syndactyly of the first webspace
- Impossible to obtain consent from parents or patients or refusal
- Unable to travel to Lille University Hospital for the consultation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
chu de Lille
Lille, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 13, 2023
First Posted
May 19, 2026
Study Start
December 7, 2023
Primary Completion
December 1, 2024
Study Completion
June 30, 2025
Last Updated
May 19, 2026
Record last verified: 2026-05