NCT07762404

Brief Summary

assess and compare the functional and aesthetic outcomes of different surgical techniques used for reconstruction of post-traumatic and post-burn first web space obliteration.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
11mo left

Started Jul 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress6%
Jul 2026Jul 2027

First Submitted

Initial submission to the registry

July 19, 2026

Completed
6 days until next milestone

Study Start

First participant enrolled

July 25, 2026

Completed
19 days until next milestone

First Posted

Study publicly available on registry

August 13, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2027

Last Updated

August 13, 2026

Status Verified

August 1, 2026

Enrollment Period

11 months

First QC Date

July 19, 2026

Last Update Submit

August 8, 2026

Conditions

Reconstruction of First Web Space

Keywords

Surgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis.

Outcome Measures

Primary Outcomes (3)

  • Functional outcome of first web space reconstruction

    Functional Assessment: Thumb-index angle measured using a goniometer during maximal thumb abduction by centimeters.

    6 months postoperative

  • Functional outcome of first web space reconstruction

    Functional Assessment: Kapandji Opposition Score

    6 months follow up

  • Functional outcome of first web space reconstrcution

    Grip strength By Handheld dynamometer.

    6 months follow up

Study Arms (1)

Reconstruction of post burn first web space obliteration in hand

EXPERIMENTAL

Patients with post-burn or post-traumatic first web space obliteration undergoing surgical reconstruction. Functional outcomes (thumb-index angle, Kapandji score, and grip strength), sensory recovery, and aesthetic outcomes will be evaluated over a 6-month follow-up period.

Procedure: Reconstruction of post burn first web space obliteration in handProcedure: First web space ReconstructionProcedure: Reconstruction of first web space

Interventions

Reconstruction of post burn first web space obliteration in handPROCEDURE

Surgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis.

Reconstruction of post burn first web space obliteration in hand
First web space ReconstructionPROCEDURE

Reconstruction of post burn first web space obliteration in hand

Reconstruction of post burn first web space obliteration in hand
Reconstruction of first web spacePROCEDURE

Reconstruction of post burn first web space obliteration in hand

Reconstruction of post burn first web space obliteration in hand

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Patients with post-burn or posttraumatic first web space contracture.Functional limitation of thumb abduction Patients medically fit for surgical intervention.

You may not qualify if:

  • Active infection in the affected hand. Uncontrolled diabetes or peripheral vascular disease Previous failed reconstruction of the same web spacel Patients unable to comply with postoperative follow-up.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sohag university hospital

Sohag, Sohag Governorate, Egypt

Location

Related Links

Central Study Contacts

Merna Mohsen Ebaid, Master degree

CONTACT

01100451332mernamohsen45@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

July 19, 2026

First Posted

August 13, 2026

Study Start

July 25, 2026

Primary Completion (Estimated)

June 15, 2027

Study Completion (Estimated)

July 15, 2027

Last Updated

August 13, 2026

Record last verified: 2026-08

Locations

EG(1)