LungTx-Lock: Comparative Study Between Sternal Closure With Sternalock® Blue Versus Steel Wire Submitted To Bilateral Anterior Transsternal Thoracotomy (Clamshell) For Bilateral Lung Transplant

Sponsor
University of Sao Paulo General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05055739
Collaborator
(none)
40
1
2
43
0.9

Study Details

Study Description

Brief Summary

This will be a prospective, randomized clinical trial, comparing the sternal alignment between the fixation with rigid plate X steel wires. Patients over 18 years of age, belonging to the lung transplant line in the State of São Paulo, who will undergo bilateral lung transplantation will be studied.

Condition or Disease Intervention/Treatment Phase
  • Device: Rigid plate X steel wires
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparative Study Between Sternal Closure With Sternalock® Blue Versus Steel Wire Submitted To Bilateral Anterior Transsternal Thoracotomy (Clamshell) For Bilateral Lung Transplant
Actual Study Start Date :
May 2, 2019
Anticipated Primary Completion Date :
Jul 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: SW

Patients undergoing sternal closure with steel wires

Device: Rigid plate X steel wires
Compare the sternal alignment between the fixation with rigid plate X steel wires.

Experimental: RP

Patients undergoing sternal closure with a rigid plate

Device: Rigid plate X steel wires
Compare the sternal alignment between the fixation with rigid plate X steel wires.

Outcome Measures

Primary Outcome Measures

  1. Sternal Alignment [1 month]

    Sternal alignment will be analyzed through cross-sections of chest computed tomography by a certified radiologist. Two parameters will be used for sternal alignment: Misalignment: Significant:> 3mm; Non-significant: ≤3mm Deviation: Grade 1: ≤50% Grade 2:> 50%

  2. Sternal Alignment [3 months]

    Sternal alignment will be analyzed through cross-sections of chest computed tomography by a certified radiologist. Two parameters will be used for sternal alignment: Misalignment: Significant:> 3mm; Non-significant: ≤3mm Deviation: Grade 1: ≤50% Grade 2:> 50%

  3. Sternal Alignment [6 months]

    Sternal alignment will be analyzed through cross-sections of chest computed tomography by a certified radiologist. Two parameters will be used for sternal alignment: Misalignment: Significant:> 3mm; Non-significant: ≤3mm Deviation: Grade 1: ≤50% Grade 2:> 50%

Secondary Outcome Measures

  1. Bone healing [1 month]

    Bone healing will be analyzed through cross-sections of chest computed tomography by a certified radiologist. • The degree of bone healing will be classified into 6 levels: 0- (A) No signs of consolidation (no clear consolidation, no union, sternal separation) (B) Minimal consolidation (sternal separation, lack of bone bridge) (C) Median consolidation (sternal separation with some trace of bone bridge, immature bone formation) (D) Moderate consolidation (partial bone connection indicating sternal stability) (E) Partial synthesis (significant bone bridge) (F) Complete synthesis (complete bone bridge)

  2. Bone healing [3 months]

    Bone healing will be analyzed through cross-sections of chest computed tomography by a certified radiologist. • The degree of bone healing will be classified into 6 levels: 0- (A) No signs of consolidation (no clear consolidation, no union, sternal separation) (B) Minimal consolidation (sternal separation, lack of bone bridge) (C) Median consolidation (sternal separation with some trace of bone bridge, immature bone formation) (D) Moderate consolidation (partial bone connection indicating sternal stability) (E) Partial synthesis (significant bone bridge) (F) Complete synthesis (complete bone bridge)

  3. Bone healing [6 months]

    Bone healing will be analyzed through cross-sections of chest computed tomography by a certified radiologist. • The degree of bone healing will be classified into 6 levels: 0- (A) No signs of consolidation (no clear consolidation, no union, sternal separation) (B) Minimal consolidation (sternal separation, lack of bone bridge) (C) Median consolidation (sternal separation with some trace of bone bridge, immature bone formation) (D) Moderate consolidation (partial bone connection indicating sternal stability) (E) Partial synthesis (significant bone bridge) (F) Complete synthesis (complete bone bridge)

  4. Pain [1 month]

    The patients' postoperative pain will be assessed according to the Pain Score (Pain Score).

  5. Pain [3 months]

    The patients' postoperative pain will be assessed according to the Pain Score (Pain Score).

  6. Pain [6 months]

    The patients' postoperative pain will be assessed according to the Pain Score (Pain Score).

  7. Time to close the Rib cage [1 month]

    Time to close the Rib cage will be measured from the insertion of the last chest drain until the total closure of the skin of the thorax.

  8. Time to close the Rib cage [3 months]

    Time to close the Rib cage will be measured from the insertion of the last chest drain until the total closure of the skin of the thorax.

  9. Time to close the Rib cage [6 months]

    Time to close the Rib cage will be measured from the insertion of the last chest drain until the total closure of the skin of the thorax.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Above 18 years of age;

  2. Belonging to the transplant queue of InCor;

  3. Eligible for sequential bilateral lung transplantation submitted to clamshell incision;

Exclusion Criteria:
  1. Patients undergoing a new surgical procedure after lung transplantation with the need to manipulate the steel wires or the sternal fixation plate other than for osteomyelitis;

  2. Intraoperative death;

  3. Patients who have undergone unilateral lung transplantation or have not undergone a clamshell incision.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Instituto do Coração - HCFMUSP São Paulo SP Brazil 05403-900

Sponsors and Collaborators

  • University of Sao Paulo General Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Paulo Manuel Pêgo Fernandes, Principal Investigator, University of Sao Paulo General Hospital
ClinicalTrials.gov Identifier:
NCT05055739
Other Study ID Numbers:
  • University of Sao Paulo
First Posted:
Sep 24, 2021
Last Update Posted:
Sep 24, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No

Study Results

No Results Posted as of Sep 24, 2021