Actively Recruiting
Can Breathing Exercise Reduce Pulmonary Complications in Rib Fractures: Randomized Prospective Study
Led by Kastamonu University · Updated on 2024-11-14
62
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate whether breathing exercises help reduce lung complications in patients with rib fractures. The study focuses on adults aged 18 to 100 who have suffered isolated chest injuries within 24 hours. Researchers want to compare lung function and the occurrence of pulmonary problems like pneumonia between two groups receiving different treatments. Participants will be randomly divided into two groups. One group will receive standard pain relief treatment using paracetamol and dexketoprofen. The other group will receive the same pain relief plus respiratory physiotherapy with a triflow device, performing breathing exercises for 8 hours a day, 10 times per hour. This approach aims to improve lung expansion and prevent complications. During the study, lung function tests measuring FEV1, FVC, and FEV1/FVC ratios will be done on days 2 and 7. Researchers will also monitor the number of participants developing pneumonia within 7 days. The trial lasts for one week, focusing on lung performance and safety. Participants’ pain scores and respiratory capacity will be tracked to assess the effects of the breathing exercises compared to routine treatment.
CONDITIONS
Brief Title
Breathing Exercise for Rib Fracture
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Isolated thoracic injury within 24 hours
- Age between 18 and 100 years
You will not qualify if you...
- Pneumothorax and hemothorax requiring intervention at admission
- Injury severity index greater than 16
- Chronic obstructive pulmonary disease (COPD) or asthma
- Extrathoracic trauma (injuries outside the chest area)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Up to 24 hours after injury
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - 7 days
Participants receive either conservative drug treatment or respiratory physiotherapy with triflow breathing exercises in addition to routine analgesics.
Daily visits during the 7-day treatment period
Trial Site Locations
Total: 1 location
1
Kastamonu University
Kastamonu, Turkey (Türkiye), 37150
Actively Recruiting
Research Team
İ
İsmail Dal, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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