sing of short arm splint for immobilization.

Not Applicable

Recruiting

• Conditions: pper limb soft tissue injuries.; Contusion of finger(s) with damage to nail; Contusion of other parts of wrist and hand; Multiple superficial injuries of wrist and hand; Other superficial injuries of wrist and hand; Superficial injury of wrist and hand, unspecified; Sprain and strain of; S60.1; S60

• Registration Number: IRCT20170105031787N1
• Lead Sponsor: Iran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Patients, who admitted in the emergency department of 7tir Hospital” in Tehran with a complaint of upper limb trauma and need splinting

Exclusion Criteria

Patients under eighteen years old and those that can not be follow up will be rolled out.
Patients who had fracture
Patients who had dislocation
Patients who had laceration needs to repair

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Swelling. Timepoint: Before intervention; one week after intervention; two weeks after intervention; three weeks after intervention. Method of measurement: Telephone or in-person interviews with patient.;Recovery time. Timepoint: every week from splinting to removal time. Method of measurement: telephone or in-person interviews with patients.;Pain. Timepoint: every week until 3 weeks from splinting. Method of measurement: telephone or in-person interviews with patients according to pain score.;Complication such as compartment syndrome, burning of skin or sore. Timepoint: every week from splinting to removal time. Method of measurement: telephone or in-person interviews with patients.