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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05482139
Other study ID # RM14763
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2004
Est. completion date July 31, 2019

Study information

Verified date July 2022
Source Waitemata District Health Board
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 718
Est. completion date July 31, 2019
Est. primary completion date July 31, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Primary surgical procedure was incisional hernia repair with mesh Exclusion Criteria: - Suture repair - Other hernia repair (not incisional) - Operation notes unavailable

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Incisional hernia repair with mesh
open or laparoscopic repairs of incisional hernia with mesh

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Waitemata District Health Board

Outcome

Type Measure Description Time frame Safety issue
Primary Post operative complications Post operative complications as per Clavien-Dindo classification 30-days post procedure
Primary Length of Hospital Stay How long patients stayed admitted to hospital after surgery 0 days - 38 days
Secondary Recurrence of hernia Did patients experience a recurrence of their hernia, if so after what period of time post operatively. 0 days - 15 years
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