A Retrospective Analysis of Incisional Hernia Repair's Postoperative Recurrence
NCT ID: NCT06102551
Last Updated: 2023-10-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
157 participants
OBSERVATIONAL
2023-03-01
2023-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Risk Factors for Poor Outcome After Epigastric and Umbilical Hernia Repair
NCT01665859
Functional Outcome After Incisional Hernia Repair: Open Versus Laparoscopic Repair
NCT00625053
Abdominal Wall Function and Quality of Life and Before and After Incisional Hernia Repair
NCT02320071
Risk Factors for Morbidity After Incisional Hernia Repairs
NCT01430676
Effect of Reoperation for Recurrence After Open Umbilical Hernia Repair
NCT01607801
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
The primary group
No interventions assigned to this group
The recurrent group
Recurrence after surgery
Recurrence after repair was the main outcome
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Recurrence after surgery
Recurrence after repair was the main outcome
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
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.
18 Years
80 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Fudan University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Zhijun Bao
Director
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
YiMing Lin
Shanghai, Shanghai Municipality, China
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
HuadongHosptialHernia01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.