Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06222333
Other study ID # KastamonuU1
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 1, 2024
Est. completion date April 1, 2026

Study information

Verified date January 2024
Source Kastamonu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Respiratory physiotherapy is routinely performed after thoracic surgery operations to increase lung expansion and prevent pulmonary complications such as atelectasis and pneumonia. It is a controversial issue whether respiratory physiotherapy reduces pulmonary complications in rib fractures. In our study, patients with rib fractures will be divided into two groups. In the control group, standard treatment consisting of routine analgesic treatments will be applied. In the other group, respiratory physiotherapy will be applied with triflu for 8 hours a day. At the end of the study, pulmonary complications in both groups will be compared.


Description:

Patients between the ages of 18 and 100 who will apply to our hospital due to rib fractures between April 2024 and April 2025 will be evaluated. Patients who meet the inclusion criteria will be included in the study. Patients will be divided into two groups using randomization blocks. Patients in the control group will receive conservative treatment consisting of paracetamol and dexketoprofen. In the other group of patients, in addition to conservative treatment, triflow breathing exercise will be applied for 8 hours a day. Respiratory function test pain scores and pulmonary complications of patients in the two groups will be compared statistically.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 62
Est. completion date April 1, 2026
Est. primary completion date April 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Isolated thoracic injury within 24 hours - Age between 18-100 Exclusion Criteria: - Pneumothorax and hemothorax requiring intervention at admission - Injury severity index >16 - COPD, Atshma - Extrathoracic trauma

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Respiratory physiotherapy
In this group of patients, in addition to routine analgesic treatment, triflow use and deep breathing training would be given by the physiotherapist. Patients in this group will do breathing exercises 8 hours a day, 10 times an hour.
Drug:
Conservative Treatment
Patients in the control group will receive conservative treatment consisting of paracetamol and dexketoprofen.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kastamonu University

Outcome

Type Measure Description Time frame Safety issue
Primary FEV1, FVC, FEV1/FVC results on day 7 FEV1, FVC, FEV1/FVC 7 days
Secondary Number of Participants with Pneumonia Clinical and radiological diagnosis of pneumonia 7 days
Secondary FEV1, FVC, FEV1/FVC results on day 2 FEV1, FVC, FEV1/FVC 2 days
See also
  Status Clinical Trial Phase
Recruiting NCT04554186 - Serratus Anterior Plane Block Versus Thoracic Paravertebral Block. N/A
Completed NCT02432456 - Ketamine Infusion Therapy for the Management of Acute Pain in Adult Rib Fracture Patients Phase 4
Not yet recruiting NCT04168710 - Ultrasound Guided Emergency Physician Performed Erector Spinae Nerve Block for Rib Fracture Analgesia Phase 1/Phase 2
Recruiting NCT04413799 - PVB vs Ketamine/Lidocaine in Rib Fracture Patients Early Phase 1
Completed NCT05770232 - Retrospectively Analyze the Risk Factors of VTE in 5774 Patients With Thoracic Trauma From 33 Hospitals in China, and Established a Risk Prediction Model
Completed NCT03305666 - Trial of Injected Liposomal Bupivacaine vs Bupivacaine Infusion After Surgical Stabilization of Rib Fractures Phase 4
Completed NCT03768193 - Deep Serratus Anterior Plane Block vs Surgically-placed Paravertebral Block for VATS Surgery N/A
Recruiting NCT05865327 - UltrasouNd-guided Percutaneous Intercostal Nerve Cryoneurolysis for Analgesia Following Traumatic Rib Fracture N/A
Completed NCT06448078 - Comparative Evaluation of External Chest Wall Fixator Treatment Effectiveness in Patients With Rib Fractures N/A
Recruiting NCT04100512 - Oscillating Positive Expiratory Pressure (OPEP) Therapy in Trauma Patients With Multiple Rib Fractures N/A
Completed NCT02608541 - Sheffield Multiple Rib Fractures Study:
Completed NCT04168996 - Individualized Discharge Planning in Patients With Rib Fracture N/A
Recruiting NCT05714631 - Lidocaine Patches in Elderly Patients With Traumatic Rib Fractures Phase 4
Recruiting NCT03619785 - US-guided SAPB for Rib Fractures in the ED Phase 4
Suspended NCT03711812 - Serratus Anterior Block and Catheter Use in Rib Fractures in the Emergency Department N/A
Completed NCT05321121 - Dexmedotomidine for Acute Pain Control in Patients With Multiple Rib FracturesRandomized Controlled Trial Phase 4
Completed NCT04863807 - A Retrospective Review of Rib Fracture Pain Management at a London Major Trauma Centre
Withdrawn NCT05069961 - Non-Inferiority Study of Erector Spinae Plane Block Compared to Thoracic Epidural in Pain Management of Rib Fractures N/A
Recruiting NCT03919916 - Serratus Plane Block With Parenteral Opioid Analgesia Versus Patient Controlled Analgesia in Rib Fractures N/A
Terminated NCT03805360 - The Erector Spinae Plane Block and Its Effect on Respiratory Status and Pain Management in Rib Fracture Patients Phase 1