NCT05482139

Brief Summary

A retrospective review of all incisional hernia repairs at North Shore Hospital (NSH), Auckland, NZ was performed between January 2004 and July 2019. Patients who had an open or laparoscopic incisional hernia repair with mesh were included in this study. Patients were retrospectively followed up from the date of their operation until the end of the study period.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
718

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2004

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2004

Completed
15.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2019

Completed
3 years until next milestone

First Submitted

Initial submission to the registry

July 16, 2022

Completed
16 days until next milestone

First Posted

Study publicly available on registry

August 1, 2022

Completed
Last Updated

August 1, 2022

Status Verified

July 1, 2022

Enrollment Period

15.6 years

First QC Date

July 16, 2022

Last Update Submit

July 28, 2022

Conditions

Incisional Hernia

Outcome Measures

Primary Outcomes (2)

  • Post operative complications

    Post operative complications as per Clavien-Dindo classification

    30-days post procedure

  • Length of Hospital Stay

    How long patients stayed admitted to hospital after surgery

    0 days - 38 days

Secondary Outcomes (1)

  • Recurrence of hernia

    0 days - 15 years

Interventions

Incisional hernia repair with meshPROCEDURE

open or laparoscopic repairs of incisional hernia with mesh

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients who had an incisional hernia repair with mesh at WDHB between January 2004 and July 2019

You may qualify if:

  • Primary surgical procedure was incisional hernia repair with mesh

You may not qualify if:

  • Suture repair
  • Other hernia repair (not incisional)
  • Operation notes unavailable

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Incisional Hernia

Interventions

Melanocyte-Stimulating Hormones

Condition Hierarchy (Ancestors)

HerniaPathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsPostoperative ComplicationsPathologic Processes

Intervention Hierarchy (Ancestors)

MelanocortinsPro-OpiomelanocortinHypothalamic HormonesPeptide HormonesHormonesHormones, Hormone Substitutes, and Hormone AntagonistsPituitary Hormones, AnteriorPituitary HormonesNeuropeptidesPeptidesAmino Acids, Peptides, and ProteinsNerve Tissue ProteinsProteins

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Non SET Surgical Registrar

Study Record Dates

First Submitted

July 16, 2022

First Posted

August 1, 2022

Study Start

January 1, 2004

Primary Completion

July 31, 2019

Study Completion

July 31, 2019

Last Updated

August 1, 2022

Record last verified: 2022-07

Data Sharing

IPD Sharing
Will not share