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Completed

NCT Number: NCT07596862

Remote Assesment of Functional Sequelae in Patients Operated for Congenital Syndactyly

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

consultation

Other

Patients will be called in for consultation in the CHU de Lille to be examined.

Primary outcomes

  1. Study of the retraction of the webspace with Withey scale

    Time frame: From 4 years to 18 years after the surgery

Secondary outcomes

  1. Evaluation of the scars with Vancouver scale.

    Time frame: From 4 years to 18 years after the surgery

Other outcomes

  1. Evaluation of the scar from the donor site of the total skin graft with Vancouver scale.

    Time frame: 4 years to 18 years after the surgery

  2. Study of the flessum with a goniometer.

    Time frame: 4 years to 18 years after the surgery

  3. Study of the clinodactyly with a goniometer.

    Time frame: 4 years to 18 years after the surgery

  4. Study of the patients and parents satisfaction with a Likert scale.

    Time frame: 4 years to 18 years after the surgery

Sponsors and collaborators

Lead sponsor

University Hospital, Lille

Other

Registry information

Official study title

Evaluation of the Gilbert Dorsal Commissural Flap in the Managment of Congenital Syndactylies

Acronym: DISTSSEQUELO

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
May 19, 2026
Registry last updated
May 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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