Percutaneous Fixation of Acute Scaphoid Fractures

June 14, 2022 updated by: Mahmoud Mohamed Mohamed Hamadouh, Sohag University

Percutaneous Trans-trapezial Fixation of Acute Scaphoid Fractures by Herbert Screw

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

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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.

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Egypt
      • Sohag, Egypt
        • Sohag University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 60 years (ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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:

  • - 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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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
Percutaneous Trans-trapezial fixation of acute Scaphoid fractures by Herbert screw

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of wrist power
Time Frame: Up to 18 months
Modified Mayo wrist score
Up to 18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sohag University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 1, 2021

Primary Completion (ACTUAL)

May 1, 2022

Study Completion (ACTUAL)

May 1, 2022

Study Registration Dates

First Submitted

February 14, 2021

First Submitted That Met QC Criteria

February 26, 2021

First Posted (ACTUAL)

March 1, 2021

Study Record Updates

Last Update Posted (ACTUAL)

June 21, 2022

Last Update Submitted That Met QC Criteria

June 14, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Soh-Med-21-2-09

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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