Trial of Operative Fixation of Fractured Ribs in Patients With Flail Chest

Sponsor
The Alfred (Other)
Overall Status
Completed
CT.gov ID
NCT00298259
Collaborator
(none)
48
1
2
62
0.8

Study Details

Study Description

Brief Summary

Background: Fracture of several ribs in more than one place as the result of trauma, leads to paradoxical movement of the chest wall and ventilatory failure. The mainstay of management in these patients has traditionally been analgesia and positive pressure ventilation to splint the chest wall and allow healing of the ribs to begin. However, this management option leads to prolonged intensive care unit (ICU) stay with increasing complication rates as patients remain on a ventilator for prolonged periods. Patients often remain on a ventilator for two to three weeks while waiting for enough rib healing to provide sufficient chest wall stability to allow the patient to take over all their breathing themselves. Until that time, patients are at risk of pneumonia and sepsis and other complications. Long term disabilities which have been reported in these patients include ongoing pain syndromes, inability to return to work, particularly manual type labour and cosmetic chest wall deformities.

An alternative treatment strategy is to operatively fix the ribs. By fixing the ribs operatively, the patient no longer requires internal pneumatic stabilization (provided by mechanical ventilation) and can be weaned from the ventilator within days rather than weeks. This can potentially lead to earlier discharge from the intensive care unit, and an avoidance of the multiple complications which arise in the ventilated patient. Rib fixation may also lead to less pain and deformity, improved mobility in the post injury phase and earlier return to work.

Hypothesis: that early operative fixation of ribs in patients presenting with flail chest secondary to trauma will result in less mechanical ventilatory requirements, earlier discharge from the intensive care unit and lower rate of complications associated with prolonged mechanical ventilation. This will lead to cost savings in the treatment of these patients.

Condition or Disease Intervention/Treatment Phase
  • Procedure: operative fixation of fractured ribs
Phase 2

Study Design

Study Type:
Interventional
Actual Enrollment :
48 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective Randomised Trial of Operative Fixation of Fractured Ribs in Patients With Flail Chest
Study Start Date :
Jan 1, 2007
Actual Primary Completion Date :
Jan 1, 2012
Actual Study Completion Date :
Mar 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: ORIF

open reduction internal fixation of fractured ribs in flail chest patients

Procedure: operative fixation of fractured ribs
ORIFof fractured ribs in flail chest patients

No Intervention: conservative management

current standard conservative management

Outcome Measures

Primary Outcome Measures

  1. Mechanical ventilation hours [open]

  2. intensive care stay hours [open]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients with multiple (>3) fractured ribs between the level of ribs 3 to 10 resulting in a paradoxical movement of the chest wall -
Exclusion Criteria:
  • age > 75 years

  • Spinal injuries which would preclude placement of the patient in a lateral decubitus position

  • Open rib fractures with soiling or infection

  • Severe head injury

  • Uncorrected coagulopathy

  • Adult respiratory distress syndrome

  • Sepsis

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Alfred Hospital Melbourne Victoria Australia 3181

Sponsors and Collaborators

  • The Alfred

Investigators

  • Principal Investigator: Silvana Marasco, FRACS, The Alfred

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Silvana Marasco, Associate Professor Silvana Marasco, The Alfred
ClinicalTrials.gov Identifier:
NCT00298259
Other Study ID Numbers:
  • 50/06
First Posted:
Mar 2, 2006
Last Update Posted:
Dec 11, 2012
Last Verified:
Dec 1, 2012
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 11, 2012