Percutaneous Fixation of Acute Scaphoid Fractures
Percutaneous Trans-trapezial Fixation of Acute Scaphoid Fractures by Herbert Screw
1 other identifier
interventional
20
1 country
1
Brief Summary
Percutaneous Trans-trapezial fixation of acute Scaphoid fractures by Herbert screw
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2021
1 active site
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
First Submitted
Initial submission to the registry
February 14, 2021
CompletedFirst Posted
Study publicly available on registry
March 1, 2021
CompletedStudy Start
First participant enrolled
April 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2022
CompletedJune 21, 2022
June 1, 2022
1.1 years
February 14, 2021
June 14, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Change of wrist power
Modified Mayo wrist score
Up to 18 months
Study Arms (1)
group (1)
OTHERgroup (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.
Interventions
Percutaneous Trans-trapezial fixation of acute Scaphoid fractures by Herbert screw
Eligibility Criteria
You may qualify if:
- \- 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).
You may not qualify if:
- \- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (1)
Sohag university hospital
Sohag, Egypt
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- resident doctor
Study Record Dates
First Submitted
February 14, 2021
First Posted
March 1, 2021
Study Start
April 1, 2021
Primary Completion
May 1, 2022
Study Completion
May 1, 2022
Last Updated
June 21, 2022
Record last verified: 2022-06