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A Prospective Randomized Controlled Study Comparing the Clinical Effects of Surgical and Non-surgical Treatment of Low Rib Fractures

Shanghai Jiao Tong University logo

Shanghai Jiao Tong University

Status

Not yet enrolling

Conditions

Rib Fracture Multiple

Treatments

Procedure: surgical stabilization of low rib fratures
Other: converstive treatment of low rib fratures

Study type

Observational

Funder types

Other

Identifiers

NCT05758870
20220815

Details and patient eligibility

About

The purpose of this study is to explore the difference between the clinical effects of surgical and non-surgical treatment for patients with low rib fracture, and to explore whether SSRF has more clinical treatment advantages in patients with low rib fracture in a randomized, controlled and prospective manner.

Enrollment

64 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with chest trauma only and unilateral low rib fractures Three rib fractures and more Displacement of the broken end of the fracture (bicortical fracture and not in the same line) Time from injury to hospital < 24 hours Age 18-70 ASA grade I-II Preoperative arterial oxygen partial pressure >60mmHg, carbon dioxide partial pressure <50mmHg The participate is volunteer in the study and sign the informed consent Pain score( Number Rating Scale, NRS) >5 under calm breathing

Exclusion criteria

  • Difficult airway History of esophageal reflux Myasthenia gravis Coagulation disorders Gastrointestinal ulcer Gastrointestinal bleeding Anesthetic drugs allergy history Asthma Chronic obstructive pulmonary disease Pregnant women

Trial design

64 participants in 2 patient groups

Research Group
Description:
surgical stabilization of low rib fracures by internal fixation
Treatment:
Procedure: surgical stabilization of low rib fratures
Controls Group
Description:
conservative treatment of low rib fractures
Treatment:
Other: converstive treatment of low rib fratures

Trial contacts and locations

0

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Central trial contact

Weiming Wu

Data sourced from clinicaltrials.gov

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