Impact of Time Interval Between Trauma and Operation on Clinical Outcome in Patients With Delayed Rib Fixation (Nonunion)
Launched by UNIVERSITY HOSPITAL, BASEL, SWITZERLAND · Jan 16, 2025
Trial Information
Current as of July 21, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how the timing of surgery affects the recovery of patients with rib fractures that haven't healed properly, a condition known as nonunion. The researchers want to find out if having surgery sooner after the injury leads to better outcomes for patients. The study is currently looking for participants aged 18 and older who have experienced rib fractures due to various causes, such as accidents, sports injuries, or medical procedures.
If you or a loved one are considering participating, you would need to sign a consent form and meet certain criteria, such as not having received treatment for your rib fracture within three weeks of the injury. Participants will be monitored throughout the study to gather information about their recovery and overall health after surgery. It's important to note that this is an observational study, meaning the researchers will observe and collect data rather than giving specific treatments. Your involvement could help improve future care for patients with similar injuries.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients who signed the study specific consent form
- • Patients aged ≥18 years at the time of informed consent
- • Patients who provided written informed consent in accordance with ICH-GCP regulations prior to participating any protocol-specific follow-up
- • Patients with at least one rib fracture caused by trauma (traffic accident, falls), surgery (cardiac, thoracic, lung transplantation), sports, cough, and cardiopulmonary resuscitation
- Exclusion Criteria:
- • Patients who were treated conservatively
- • Patients who underwent rib fixation till 3 weeks after trauma
- • Patients who underwent SSRF prior to SSRFN
- • Patients who are unable to follow the procedures of the study, e. g. have insufficient knowledge of German or French languages, psychological disorders, dementia etc.
- • Patients with a pathological rib fracture(s) due to malignancy or radiation
- • Participation in any interventional study in our department that might influence any of the outcome parameters
- • Patients who underwent an initial surgery of rib fracture prior to development of a rib fracture nonunion
About University Hospital, Basel, Switzerland
The University Hospital Basel, Switzerland, is a leading academic medical center renowned for its commitment to cutting-edge research and innovative patient care. As a prominent clinical trial sponsor, the hospital leverages its extensive expertise and state-of-the-art facilities to advance medical knowledge and therapeutic options across various disciplines. With a collaborative approach that integrates clinical practice and scientific inquiry, the University Hospital Basel fosters an environment conducive to rigorous clinical trials, ensuring the highest standards of safety and efficacy. Its strategic focus on patient-centered research aims to translate scientific discoveries into tangible health solutions, benefiting both local and global communities.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Basel, Basel Stadt, Switzerland
Patients applied
Trial Officials
Maria Svec
Principal Investigator
Department of Thoracic Surgery, University Hospital Basel
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported