Sternal Closure in Children After Cardiac Surgery

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05715060
Collaborator
(none)
45
1
2
21.1
2.1

Study Details

Study Description

Brief Summary

comparison between stainless steel wires and PDS in closure of sternum in children after cardiac surgery in terms of sternal dehiscence, infection & cosmetic outcome

Condition or Disease Intervention/Treatment Phase
  • Procedure: Median sternotomy closure (sternal closure)
N/A

Detailed Description

Median sternotomy is considered to be the gold standard incision in cardiac surgery. Sternotomy has to be performed properly to avoid short- and long-term morbidity and mortality. The surgical technique is well established and certain principles are recognized to be crucial to minimize complications. The identification of the correct landmarks, midline tissue preparation, osteotomy with the avoidance of injury to underlying structures like pleura, pericardium and ectatic ascending aorta, and targeted bleeding control are important steps of the procedure. As important as the performance of a proper sternotomy is a correct sternal closure. An override or shift of the sternal edges has to be avoided by placing the wires at a proper distance from each other without injuring the thoracic pedicle. The two sternal halves have to be tightly re-approximated to facilitate healing of the bone and to avoid instability, which is a risk factor for wound infection. With a proper performance of sternotomy and sternal closure, instability and wound infections are rare and depend on patient-related risk factors . Conventional closure uses stainless steel wire sutures which may not be the ideal approach as sternal wound infection and mediastinitis are troublesome complications following this method which are major causes of morbidity and mortality of patients. Availability of delayed absorbable sutures such as polydioxanone sutures (PDS) for sternal closure allows us to test the efficacy of it in prevention of these complications.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
45 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Stainless Steel Wire vs. Polydioxanone "PDS" at Sternal Closure in Children After Cardiac Surgery
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: stainless steel wire closure

conventional closure of median sternotomy by stainless steel wire

Procedure: Median sternotomy closure (sternal closure)
Comparison of Sternal closure after cardiac surgery between conventional way which is by stainless steel wire & Polydioxanone (PDS)

Active Comparator: PDS sternal closure

closure of median sternotomy by PDS

Procedure: Median sternotomy closure (sternal closure)
Comparison of Sternal closure after cardiac surgery between conventional way which is by stainless steel wire & Polydioxanone (PDS)

Outcome Measures

Primary Outcome Measures

  1. Sternal stability [up to 2 years]

    Comparison of incidence of sternal dehiscence & instability between 2 groups this is done by clinical assessment(history & examination) & follow up chest x-rays

Secondary Outcome Measures

  1. cosmetic outcome (prominent wire) [up to 2 years]

    calculation and observation of prominent wire incidence in patients closed with stainless steel wire Done by clinical assessment(history & examination)

  2. Wound infection [up to 2 years]

    comparison of incidence of skin infection between 2 groups Done by clinical assessment(history & examination)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 5 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Infants & children up to 5 years old underwent open heart surgery in Assiut University heart hospital
Exclusion Criteria:
  • Older than 5 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assiut University heart hospital Assiut Egypt 71511

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mostafa Ibrahim Mohammad AbdelHafeez, Resident, Assiut University
ClinicalTrials.gov Identifier:
NCT05715060
Other Study ID Numbers:
  • sternal closure in children
First Posted:
Feb 6, 2023
Last Update Posted:
Feb 6, 2023
Last Verified:
Feb 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Feb 6, 2023