Reconstruction of First Web SpaceNCT07762404
Reconstruction of First Web Space After Trauma and Burn
A study testing Reconstruction of post burn first web space obliteration in hand, First web space Reconstruction and Reconstruction of first web space in people with Reconstruction of First Web Space, run by Sohag University at 1 site in Egypt.
Trial 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. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Reconstruction of First Web Space
- What is being tested?
- Reconstruction of post burn first web space obliteration in hand, First web space Reconstruction and Reconstruction of first web space
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteEgypt
- Study dates
- 25 Jul 2026to 15 Jul 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Patients with post-burn or posttraumatic first web space contracture.Functional limitation of thumb abduction Patients medically fit for surgical intervention.
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Surgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis.
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.
Read the detailed description
This prospective comparative clinical study will be conducted on patients presenting with first web space contracture secondary to trauma or burn injury at the Department of Plastic Surgery, Sohag University Hospital.
Follow-up:
After reconstructive surgery patients will be reviewed at one month, 3 months and 6 months postop
- Conditions
- Reconstruction of First Web Space
- Being tested
- Reconstruction of post burn first web space obliteration in hand, First web space Reconstruction, Reconstruction of first web space
- Keywords
- Surgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis.
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Reconstruction of post burn first web space obliteration in handProcedure or surgery
Surgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis.
First web space ReconstructionProcedure or surgery
Reconstruction of post burn first web space obliteration in hand
Reconstruction of first web spaceProcedure or surgery
Reconstruction of post burn first web space obliteration in hand
| Study group | Role | What they receive |
|---|---|---|
| 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. Receives: Procedure: Reconstruction of post burn first web space obliteration in hand; Procedure: First web space Reconstruction; Procedure: Reconstruction of first web space |
What is being measured
The primary outcome is the main question the study is designed to answer.
Functional outcome of first web space reconstruction
Functional Assessment:
Thumb-index angle measured using a goniometer during maximal thumb abduction by centimeters.
Measured: 6 months postoperative
Functional outcome of first web space reconstruction
Functional Assessment:
Kapandji Opposition Score
Measured: 6 months follow up
Functional outcome of first web space reconstrcution
Grip strength By Handheld dynamometer.
Measured: 6 months follow up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Aug 2026
- Study start25 Jul 2026 (estimated)
- Primary completion15 Jun 2027 (estimated)
- Study completion15 Jul 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Reconstruction of First Web SpaceStudies of the same condition, open and under way.
- More trials run by Sohag UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Sohag University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Merna Mohsen Abeed, Sohag University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07762404
- Sponsor's protocol ID
- Soh_Med_26_6_8MS
- Status last verified
- Aug 2026
- First submitted
- 19 Jul 2026
- Last updated
- 13 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 13 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Surgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis.
- ClinicalTrials.gov ID
- NCT07762404
- Acronym / sponsor ID
- Soh_Med_26_6_8MS
- Conditions
- Reconstruction of First Web Space
- Keywords
- Surgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis.
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- Sohag UniversityUniversity, hospital or other
- Study start
- 25 Jul 2026 (estimated)
- Primary completion
- 15 Jun 2027 (estimated)
- Study completion
- 15 Jul 2027 (estimated)
- First posted
- 13 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
This prospective comparative clinical study will be conducted on patients presenting with first web space contracture secondary to trauma or burn injury at the Department of Plastic Surgery, Sohag University Hospital.
Follow-up:
After reconstructive surgery patients will be reviewed at one month, 3 months and 6 months postop
Study design
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Reconstruction of post burn first web space obliteration in hand | Experimental | Procedure: Reconstruction of post burn first web space obliteration in hand, Procedure: First web space Reconstruction, Procedure: Reconstruction of first web spacePatients 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. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- Patients with post-burn or posttraumatic first web space contracture.Functional limitation of thumb abduction Patients medically fit for surgical intervention.
Key exclusion criteria (1 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Reconstruction of post burn first web space obliteration in handSurgical Reconstruction of Post-Traumatic and Post-Burn First Web Space Obliteration: Functional and Aesthetic Outcome Analysis. | Procedure or surgery | Reconstruction of post burn first web space obliteration in hand |
| First web space ReconstructionReconstruction of post burn first web space obliteration in hand | Procedure or surgery | Reconstruction of post burn first web space obliteration in hand |
| Reconstruction of first web spaceReconstruction of post burn first web space obliteration in hand | Procedure or surgery | Reconstruction of post burn first web space obliteration in hand |
Primary outcome
Functional outcome of first web space reconstruction
Time frame: 6 months postoperative
Functional Assessment: Thumb-index angle measured using a goniometer during maximal thumb abduction by centimeters.
Functional outcome of first web space reconstruction
Time frame: 6 months follow up
Functional Assessment: Kapandji Opposition Score
Functional outcome of first web space reconstrcution
Time frame: 6 months follow up
Grip strength By Handheld dynamometer.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Aug 2026.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Reconstruction of post burn first web space obliteration in hand, First web space Reconstruction and Reconstruction of first web space in people with Reconstruction of First Web Space, run by Sohag University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 13 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Merna Mohsen Ebaid, Master degree (01100451332, mernamohsen45@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Functional outcome of first web space reconstruction (time frame: 6 months postoperative). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Aug 2026.