Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
ID06222333

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

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Isolated thoracic injury within 24 hours
  • Age between 18 and 100 years
Not Eligible

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

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Your Study Journey

Screening

Duration - Up to 24 hours after injury

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Treatment

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

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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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