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CompletedNCT04776551Updated Jun 21, 2022

Percutaneous Fixation of Acute Scaphoid Fractures

An interventional study of Percutaneous fixation of acute Scaphoid fractures in Scaphoid Fracture, sponsored by Sohag University. Completed at 1 site in Egypt. Open to participants aged 16 Years to 60 Years. Per ClinicalTrials.gov, last updated 2022-06-21.

Sponsored by Sohag University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
16 Years to 60 Years
Sex
All
01

Study summary

Percutaneous Trans-trapezial fixation of acute Scaphoid fractures by Herbert screw

Read the detailed description

Aim of the work:

To assessment outcomes of percutaneous Trans-trapezial fixation of acute scaphoid fracture.

Operative Technique:

Anesthesia: carried out under general anesthesia or brachial plexus block and under tourniquet control.

Position: supine. Approach: Percutaneous Trans-trapezial fixation of acute Scaphoid fracture. Recording any intraoperative complication that may affect the result.

Postoperative Follow Up:

Short arm circular cast including the thumb will be applied. After 3 weeks, cast will be removed and exercises will start.

02

Conditions studied

  • Scaphoid Fracture
03

In context

Lead sponsor

Sohag University is the lead sponsor of 1,220 studies on the registry; 629 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • - Acute stable non displaced waist fracture (A2).
  • Acute unstable oblique distal third (B1).
  • Acute unstable displaced waist (B2).
  • Acute un stable fracture dislocation (B4).
  • Acute un stable comminuted fracture (B5).

Exclusion criteria

Exclusion Criteria:

  • - Acute stable fracture tubercle (A1).
  • Acute unstable fracture proximal pole (B3).
  • Delayed union fracture (C).
  • Established non-union fracture includes fibrous (D1) and sclerotic (D2).
  • Bilateral fractures because of possible interference with postoperative grip strength measurement.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Other
    group (1)

    group (1) who are complaining of acute scaphoid fractures,we will do percutaneous trans trapezial fixation of scaphoid by Herbert screw.Short arm circular cast including the thumb will be applied. After 3 weeks, cast will be removed and exercises will start.

    Procedure: Percutaneous fixation of acute Scaphoid fractures

Interventions

  • ProcedurePercutaneous fixation of acute Scaphoid fractures

    Percutaneous Trans-trapezial fixation of acute Scaphoid fractures by Herbert screw

06

What researchers measure

Primary outcomes

  1. Change of wrist power

    Modified Mayo wrist score

    Time frame: Up to 18 months

07

Study locations

1 site
  • Sohag university hospital
    Sohag, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 21, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04776551
Lead sponsor
Sohag University
Responsible party
Mahmoud Mohamed Mohamed Hamadouh (resident doctor, Sohag University) — Principal investigator
First posted
Mar 1, 2021
Start date
Apr 1, 2021
Primary completion
May 1, 2022
Completion
May 1, 2022
Last update
Jun 21, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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