- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06222320
Kinesiotaping Method for Rib Fractures
October 8, 2024 updated by: İsmail DAL, Kastamonu University
Can Kinesiotaping Reduce Pain in Rib Fractures?: Randomized Prospective Study
Kinesiotaping is used as a physiotherapy method to reduce muscle pain.
In this technique, kinesiotaping tapes are attached to the relevant parts of the body.
Patients experience serious pain in rib fractures.
Kinesiotaping technique can potentially reduce pain by contributing to external stabilization of the ribs.
In this study, patients with isolated rib fractures will be divided into two groups.
The first group will be treated with kinesiotaping technique and routine painkillers.
The second group will receive routine painkiller treatment.
Pain scores between both groups will be compared.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
34
Phase
- Phase 2
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Kastamonu, Turkey, 37150
- Kastamonu University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Isolated thoracic injury within the last 24 hours
- Patients aged 18-100 years
Exclusion Criteria:
- Hemothorax and pneumothorax requiring intervention
- Injury severity index>16
- Asthma and COPD
- Tape allergy
- Loss of consciousness (GCS <15)
- Incapacitated patients
- Fracture of rib number 1-3
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Kinesiotaping group
Kinesiotaping will be applied to patients in this group in addition to painkillers.
|
Kinesiotaping will be applied to patients in this group in addition to painkillers.
Kinesiotaping is a physical therapy technique used to treat muscle pain.
It is performed with kinesiotaping tapes attached to the skin.
These bands are removed after 4-5 days.
Other Names:
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Active Comparator: Routine treatment group
Patients in this group will be administered painkillers routinely in the hospital.
|
Patients in this group will be treated with painkillers consisting of paracetamol and dexketoprofen.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Day 4 Visual Analogue Scale Pain Score
Time Frame: 4 days
|
Visual analog scale pain score on the 4th day after rib fracture
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4 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 24, 2024
Primary Completion (Actual)
October 1, 2024
Study Completion (Actual)
October 1, 2024
Study Registration Dates
First Submitted
January 3, 2024
First Submitted That Met QC Criteria
January 15, 2024
First Posted (Actual)
January 24, 2024
Study Record Updates
Last Update Posted (Estimated)
October 9, 2024
Last Update Submitted That Met QC Criteria
October 8, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pain
- Neurologic Manifestations
- Wounds and Injuries
- Thoracic Injuries
- Chest Pain
- Fractures, Bone
- Rib Fractures
- Physiological Effects of Drugs
- Peripheral Nervous System Agents
- Sensory System Agents
- Anti-Inflammatory Agents, Non-Steroidal
- Analgesics, Non-Narcotic
- Anti-Inflammatory Agents
- Antirheumatic Agents
- Analgesics
- Dexketoprofen trometamol
Other Study ID Numbers
- KastamonuU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Yes
IPD Sharing Time Frame
Data will become available persistantly on 1.4.2025.
IPD Sharing Access Criteria
Upon reasonable request principal investigator will share the data.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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