Changes in Function of the Upper Limb With Physiotherapy

NCT ID: NCT06139731

Last Updated: 2025-01-27

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

17 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-01

Study Completion Date

2026-01-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This paper describes a pilot clinical study designed to compare changes in ROM, muscle strength and functional recovery of the upper limb during the inpatient treatment period of burn injury.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Patients with burns can face challenges throughout their recovery, including contractures and a reduced range of motion (ROM) in the upper limb (UL), upper and lower limb impairment. Restoring range of motion, muscle strength, and mobility is essential to reduce scarring formation and contractures. The study included 17 patients with unilateral or bilateral superficial, deep partial and full thickness burns to the upper limbs, with or without burns to the upper body, covering 10% or more of the total body surface area

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Burn of Upper Limb, Except Wrist and Hand

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* patients aged 18-69 years
* had burns on the upper limb(s) with or without burns on the upper body
* burns involving ≥ 10% total body surface area (TBSA) with the presence of deep partial thickness or full thickness burns
* who agreed to take part in the study

Exclusion Criteria

* inability to perform or understand tests
* other injuries (fractures, brain injury)
* central and peripheral nervous system disorders
* amputation
* with burns on the head, hands, feet, and genital area
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Lithuanian University of Health Sciences

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Brigita Siparyte-Sinkeviciene

Brigita Siparyte-Sinkeviciene

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Rytis Rimdeika, Prof

Role: PRINCIPAL_INVESTIGATOR

Lithuania LUHS hospital Kaunas Clinics, Department of Plastic and Reconstructive Surgery

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Brigita Siparytė-Sinkevičienė

Kaunas, , Lithuania

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Lithuania

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Brigita Siparytė-Sinkevičienė

Role: CONTACT

+37068294149

Rytis Rimdeika, Prof

Role: CONTACT

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Brigita Siparytė-Sinkevičienė

Role: primary

+37068294149

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Brigita Siparyte-Sinkeviciene

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.