Fixation of Comminuted Distal Radius Fracture

NCT ID: NCT04798846

Last Updated: 2022-06-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-01

Study Completion Date

2022-04-01

Brief Summary

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comparison between different methods in fixation of comminuted distal radius fractures

Detailed Description

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This clinical study aims at comparison of treatment outcomes of Spanning plate versus spanning External fixator in fixation of comminuted distal radius fracture.

The primary outcomes that we like to measure are pain, healing. Stiffness and range of motion .

Conditions

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Distal Radius Fracture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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External fixator

patient treated by external fixator

Group Type ACTIVE_COMPARATOR

dorsal plating

Intervention Type PROCEDURE

Spanning Plate inserted dorsally below tendons Spanning External Fixator by rods inserted in distal radius and metacarpals

Dorsal plate

patient treated by dorsal spanning plate

Group Type ACTIVE_COMPARATOR

dorsal plating

Intervention Type PROCEDURE

Spanning Plate inserted dorsally below tendons Spanning External Fixator by rods inserted in distal radius and metacarpals

Interventions

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dorsal plating

Spanning Plate inserted dorsally below tendons Spanning External Fixator by rods inserted in distal radius and metacarpals

Intervention Type PROCEDURE

Other Intervention Names

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External fixator

Eligibility Criteria

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Inclusion Criteria

* Skeletally mature patients aging 18 or more
* Comminuted distal radius fractures Fernandez type V

Exclusion Criteria

* Age less than 18 year or more
* Patients with previous fracture affecting wrist joint in the same side.
* Parients with active infection in the affected joint
* Pathological fracture
* Neurological disorder (epilepsy…etc) Reheumatoid
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Sohag University

OTHER

Sponsor Role lead

Responsible Party

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Eslam Abdelnaby Abdelsabor

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Sohag University Hospital

Sohag, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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Soh_Med_21_02_11

Identifier Type: -

Identifier Source: org_study_id

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