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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02635165
Other study ID # 2014-A01844-43
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 2015
Est. completion date December 2020

Study information

Verified date April 2019
Source Poitiers University Hospital
Contact Christophe CJ JAYLE, PI
Phone 05.49.44.30.07
Email christophe.jayle@chu-poitiers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Optimize the management of polytraumatises with flail chest: surgical treatment Stracos by decreasing the length of stay and the late complications: pain chronicles, quality of life, respiratory function


Recruitment information / eligibility

Status Recruiting
Enrollment 310
Est. completion date December 2020
Est. primary completion date November 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients with flail chest including bifocal fracture of three or more consecutive ribs in at least two places with or without paradoxical movement

- The surgical procedure was performed in the first 48 hours after admission

- pathology with prognosis for survival 6-month-old inferior

Exclusion Criteria:

- Paraplegia or Tetraplegia

- Patients having the necessity of neurosurgical treatment or reanimation of neurosurgical

- Aorta hematoma or rupture

- ß-HCG positive in women

- titanium allergy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Thoracic osteosyntheses with Stracos


Locations

Country Name City State
France Hospital University of Poitiers Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Average cost hospitalization Average cost hospitalization without the intensive care cost.The cost of the hospitalization will be calculated by adding the cost of the surgery and hospital stay- time of the surgery-The number of Stracos used by patient 4 weeks
Secondary length of hospital stays of the intensive care department From the first day to the last day in the intensive care department. Care department - monitoring patients with traumatic hemothorax - lung pulmonary infectious associated - 4 weeks
Secondary length of hospital stays From the first day to the last day in the hospital 4 weeks
Secondary occurence of pulmonary infection 12 months of follow up
Secondary The vital capacity (VC) Volume measurement (L) visit 3 months, visit 6 months, visit 12 months after the surgery
Secondary The expiratory reserve volume (ERV) Volume measurement (L) visit 3 months, visit 6 months, visit 12 months after the surgery
Secondary The total lung capacity (TLC) Volume measurement (L) visit 3 months, visit 6 months, visit 12 months after the surgery
Secondary Residual volume (RV) Volume measurement (L) visit 3 months, visit 6 months, visit 12 months after the surgery
Secondary 6 min walk test (6MWT) Distance measurement (M) visit 3 months, visit 6 months, visit 12 months after the surgery
Secondary Visual analog scorer for pain at visit 7 days, 28 days, 3 months, 6 months and 12 months
Secondary Patient Global Assessment to measure quality of life at visit 7 days, 28 days, 3 months, 6 months and 12 months
Secondary date of return to work visit 3 months, 6 months and 12 months