ClinicalTrials.gg
RecruitingNCT06222333Updated Nov 14, 2024

Breathing Exercise for Rib Fracture

An interventional study of Respiratory physiotherapy and Conservative Treatment in Rib Fractures and Spirometry, sponsored by Kastamonu University. Recruiting at 1 site in Turkey. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2024-11-14.

Sponsored by Kastamonu University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by Apr 2025, 1 year 7 months ago, but the record still lists the study as recruiting.
  • Started Nov 2024; still recruiting 1 year 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
62
Allocation
Randomized
Ages
18 Years to 100 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 13 studies in Rib Fractures with a site in Turkey — 3 open to participants now, 4 under way, none of them phase 3. Rib Fractures · Turkey.

Planned enrollment
6th of 12
62 · median 61
Started
2024
with 3 others
No phase
8 of 13
3 open now
Registered
4th of 13
by date
Lead sponsor
2 of 13
Kastamonu University

Among the 13 studies in Rib Fractures with a site in Turkey, this one is the 6th largest by planned enrollment of the 12 interventional ones that give a count, is one of 4 that started in 2024, is one of 8 with no phase, and was the 4th registered.

Rib Fractures

126 studies on the registry are indexed under Rib Fractures; 28 are open to participants now.

This study's planned enrollment of 62 is close to the median of 60 across 92 interventional studies indexed under Rib Fractures.

Browse Rib Fractures studies →

Open to participants now

3 of the 13 studies in Rib Fractures with a site in Turkey are open now, in 1 country. Each count lists the studies.

All 3 open studies →

Where they have run

Who these studies take

Of the 13 Rib Fractures studies recruiting now, 9 (69%) set no upper age limit and 1 (8%) stop at 75 or younger; 0 take children under 18; 2 take healthy volunteers.

This study: 18 Years to 100 Years · all sexes · no healthy volunteers.

The full table on the hub →
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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 13 studies in Rib Fractures with a site in Turkey, or all of them as a file.
02

Study 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.

Read the detailed 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.

03

Conditions studied

  • Rib Fractures
  • Spirometry

Browse trials for

04

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Isolated thoracic injury within 24 hours
  • Age between 18-100

Exclusion criteria

Exclusion Criteria:

  • Pneumothorax and hemothorax requiring intervention at admission
  • Injury severity index >16
  • , Atshma
  • Extrathoracic trauma
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
62 participants (estimated)

Study arms

  • Experimental
    Respiratory physiotherapy group

    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

    Behavioral: Respiratory physiotherapy

  • Active comparator
    Routine treatment group

    Patients in the control group will receive conservative treatment consisting of paracetamol and dexketoprofen.

    Drug: Conservative Treatment

Interventions

  • BehavioralRespiratory 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.

    Also known as: Triflow

  • DrugConservative Treatment

    Patients in the control group will receive conservative treatment consisting of paracetamol and dexketoprofen.

    Also known as: Control

06

What researchers measure

Primary outcomes

  1. FEV1, FVC, FEV1/FVC results on day 7

    FEV1, FVC, FEV1/FVC

    Time frame: 7 days

Secondary outcomes

  1. Number of Participants with Pneumonia

    Clinical and radiological diagnosis of pneumonia

    Time frame: 7 days

  2. FEV1, FVC, FEV1/FVC results on day 2

    FEV1, FVC, FEV1/FVC

    Time frame: 2 days

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Yes

Time frame: Data will be available permanently on 1.4.2025

Access criteria: Upon reasonable request principal investigator will share date

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Nov 2024 (actual). Primary completion is estimated for Apr 2025, 4 months after the start.

Of 40 non-industry interventional studies with no phase under Rib Fractures, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 37. This study's planned 4 months is below that.

Counting every sponsor, half of 40 studies reached it within 23 months; a quarter within 15 and three quarters within 37.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 3, 2024
First posted
Jan 24, 2024
StartActual
Nov 13, 2024
Primary completionEst.
Apr 1, 2025
CompletionEst.
Apr 1, 2026
Last update
Nov 14, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 14, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06222333
Lead sponsor
Kastamonu University
Responsible party
İsmail DAL (Assistant Professor Literally: Doctor Teaching Member, Kastamonu University) — Principal investigator
First posted
Jan 24, 2024
Start date
Nov 13, 2024
Primary completion
Apr 1, 2025 (estimated)
Completion
Apr 1, 2026 (estimated)
Last update
Nov 14, 2024

Study contacts

İsmail Dal, MD
Contact
drismaildal@gmail.com
+905446533224

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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