NCT04776551

Brief Summary

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

Trial Health

87
On Track

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
Completed

Started Apr 2021

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
15 days until next milestone

First Posted

Study publicly available on registry

March 1, 2021

Completed
1 month until next milestone

Study Start

First participant enrolled

April 1, 2021

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2022

Completed
Last Updated

June 21, 2022

Status Verified

June 1, 2022

Enrollment Period

1.1 years

First QC Date

February 14, 2021

Last Update Submit

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)

OTHER

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

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

group (1)

Eligibility Criteria

Age16 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

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

Study Sites (1)

Sohag university hospital

Sohag, Egypt

Location

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

Locations