A Retrospective Analysis of Incisional Hernia Repair's Postoperative Recurrence
Sponsor
Fudan University (Other)
Overall Status
Completed
CT.gov ID
NCT06102551
Collaborator
(none)
157
1
6
26.1
Study Details
Study Description
Brief Summary
ABSTRACT Purpose:A retrospective study was conducted among patients with incisional hernia in our hospital to analyse the factors associated with postoperative recurrence of abdominal wall incisional hernia.
Methods:Patients with a diagnosis of incisional hernia obtained from our hospital's electronic medical record system were divided into primary incisional hernia group and recurrent incisional hernia group according to whether or not they had a recurrence after surgery. Baseline information on these patients was recorded and statistically analysed after our review.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
157 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
A Retrospective Study of Factors Associated With Postoperative Recurrence of Incisional Hernia Repair in the Abdominal Wall
Actual Study Start Date
:
Mar 1, 2023
Actual Primary Completion Date
:
Jul 1, 2023
Actual Study Completion Date
:
Aug 31, 2023
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
The primary group
|
|
The recurrent group
|
Behavioral: Recurrence after surgery
Recurrence after repair was the main outcome
|
Outcome Measures
Primary Outcome Measures
- Recurrent [2017.1-2023.8]
Recurrence after surgery repair
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- Inclusion criteria: diagnosis of incisional hernia of the abdominal wall and primary; surgical treatment for hernia repair at our hospital; all patients originating from outpatient clinics rather than emergency clinics; age of 18 to 80 years at the time of admission; and those with a well-established preoperative examination.
Exclusion Criteria:
- Exclusion criteria: severe organ dysfunction (ASA score of IV, V, VI); unconsciousness and poor cooperation with various preoperative examinations; correction of other types of abdominal hernia by perfect examination after admission; incomplete necessary information.
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | YiMing Lin | Shanghai | Shanghai | China | 000000 |
Sponsors and Collaborators
- Fudan University
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Zhijun Bao,
Director,
Fudan University
ClinicalTrials.gov Identifier:
NCT06102551
Other Study ID Numbers:
- HuadongHosptialHernia01
First Posted:
Oct 26, 2023
Last Update Posted:
Oct 26, 2023
Last Verified:
Oct 1, 2023
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
Additional relevant MeSH terms: