Wire vs Prolen: Is the Use of Prolene as Sufficient as the Use of Wire in Shouldice Surgery to Keep the Recurrence Rate Low After One Year?

Sponsor
Shouldice Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05879770
Collaborator
(none)
1,400
1
6
234.1

Study Details

Study Description

Brief Summary

When conducting the Shouldice procedure the 4-layer suture of the transversalis fascia is usually done with Prolene worldwide. At the Shouldice hospital the wire has originally been used for these augmentation. During the last decade several Shouldice Surgeons started to use the Prolene due to occasional delivery problems of the wire from Germany.

The 1-year- recurrence rate at the Shouldice hospital is 1,15% (mainly wire-use). The published 1-year recurrence rate in Europe is 2%.

As quality assessment, this project intends to evaluate these two options for suturing (wire vs Prolene) in the elective inguinal hernia patient in terms of 1-year recurrence rate. The population of focus will be those who had a primary or secondary inguinal hernia operation at Shouldice Hospital and the project is estimated to take 3 months.

Condition or Disease Intervention/Treatment Phase
  • Other: suture material

Detailed Description

  1. Study design A total of 1400 patients (n=700 with wire; n=700 with Prolene) who underwent Shouldice surgery at Shouldice Hospital will be contacted by telephone. They will be asked whether a relapse occurred after their surgery.
Sample size calculation:

The 1-year recurrence rate at Shouldice Hospital is 1.15% (mainly wire use). The published 1-year recurrence rate in Europe is 2% [1-3]. Statistics: non-inferiority: delta for non-inferiority (defined equivalence range) = 1%. Total N = 1120 (0% dropout), with 20% dropout: N = 1400.) The same number of patients will be analyzed with regard to Shouldice repair due to a first relapse (time period of data extraction 2019-2021).

Since over 6000 hernias are operated annually, a consecutive data extraction of patients operated in 2021 will be performed.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1400 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Is the Use of Prolene as Sufficient as the Use of Wire in Shouldice Surgery to Keep the Recurrence Rate Low After One Year?
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Jan 1, 2024
Anticipated Study Completion Date :
Mar 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Wire group

Patients who underwent Shouldice inguinal hernia repair using wire.

Other: suture material
Some patients have had a shouldice repair with wire in the past and others with Prolene.

prolene group

Patients who underwent Shouldice inguinal hernia repair using prolene.

Other: suture material
Some patients have had a shouldice repair with wire in the past and others with Prolene.

Outcome Measures

Primary Outcome Measures

  1. Recurrence rate [1 year]

    One-year recurrence rate

Secondary Outcome Measures

  1. Reoperation rate due to a recurrence [1 year]

    Reoperation rate due to a recurrence

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adult patients of all sexes who have undergone inguinal hernia surgery in Shouldice technique.
Exclusion Criteria:
  • Hernia repair using a mesh

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shouldice Hospital Thornhill Ontario Canada L3T 4A3,

Sponsors and Collaborators

  • Shouldice Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shouldice Hospital
ClinicalTrials.gov Identifier:
NCT05879770
Other Study ID Numbers:
  • #2023-02
First Posted:
May 30, 2023
Last Update Posted:
May 30, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Shouldice Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 30, 2023