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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06276218
Other study ID # PSU
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2022
Est. completion date February 16, 2024

Study information

Verified date February 2024
Source Prince of Songkla University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized control trial was conducted to compare the outcomes of conservative management for closed midshaft clavicular fractures using self-adjustable clavicular brace and standard clavicular brace.


Description:

Ten patients aged 18-75 years with midshaft clavicle fractures were enrolled in the study during February 2022 to February 2023. 6 patients were managed with standard clavicular brace and 4 patients with self-adjustable clavicular brace. All patients were scheduled for follow-up appointments at 1 week, 2 weeks, 4 weeks, 6 weeks and 12 weeks. Results were assessed based on clinical, functional and radiographic outcomes using the DASH questionnaire, pain, measured by VAS, analgesic usage, displacement, shortening, time to union, and patient satisfaction,


Recruitment information / eligibility

Status Recruiting
Enrollment 68
Est. completion date February 16, 2024
Est. primary completion date February 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Patient with aged between 18 - 75 years old - Closed isolated fracture midshaft of clavicle within 9 days after the injury date Exclusion Criteria: - After bracing, fracture displacement and/or shortening > 2 cm or fracture comminution > 3 fragments - Segmental fracture - Open fracture - Impending open fracture (soft tissue compromise/skin lesion) - Ipsilateral upper extremities fracture which disturbs clavicular bracing - Floating shoulder which surgical treatment is indicated. - Patients with other injuries (e.g. head injury, chest and abdomen injury) which interrupted clavicular bracing - Pathologic fracture - Patient has limitation for clavicular brace application - Pregnant women

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Clavicular brace
Clavicular brace for conservative treatment of closed midshaft clavicular fractures

Locations

Country Name City State
Thailand Prince of Songkla University Songkla Hatyai

Sponsors (1)

Lead Sponsor Collaborator
Prince of Songkla University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary DASH DISABILITIES OF THE ARM, SHOULDER AND HAND 1, 2, 4, 6, 12 week
Secondary Pain, analgesic usage, radiographic outcomes, time to union, and patient satisfaction Pain, analgesic usage, radiographic outcomes, time to union, and patient satisfaction 1, 2, 4, 6, 12 week
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