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CompletedNCT07790952Updated Nov 10, 2026

Predictors of Mesh Infection After Open Incisional Hernioplasty

An observational study in Predictor of Mesh Condition, sponsored by Sargodha Medical College. Completed at 1 site in Pakistan. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Sargodha Medical College · Observational

Updated Nov 10, 2026Primary completion movedStudy completion movedGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
62
Sex
All
01

Study summary

To determine the frequency of mesh infection in patient with open Incisional hernioplasty and to compare factors contributing with and without mesh infection

Read the detailed description

This prospective observational study will evaluate predictors of mesh infection following open incisional hernioplasty. Eligible patients with incisional hernia undergoing open mesh repair will be consecutively enrolled at the Department of Surgery, Dr. Faisal Masood Teaching Hospital, Sargodha. Demographic, clinical, anthropometric, and relevant perioperative factors will be recorded using a structured data collection form.

Patients will be followed postoperatively at 1 month, 3 months, and 1 year to assess the development of mesh infection and other related outcomes. Patients who develop mesh infection will be compared with those who remain infection-free to identify significant predictors. Data will be analyzed using SPSS version 26, with appropriate statistical tests and logistic regression to determine independent predictors of mesh infection.

02

Conditions studied

  • Predictor of Mesh Condition
03

In context

Lead sponsor

Sargodha Medical College is the lead sponsor of 13 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patient of all age group and both genders with Incisional hernia undergoing open mesh hernioplasty will be consecutively enrolled and followed postoperative to access the development of mesh infection and associated predictors

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. All age group patient will be included
  2. Both genders will be involved in this study
  3. Incisional hernia as per operational definition

Exclusion criteria

Exclusion Criteria:

  1. Co- Morbid condition including hypertension, Tuberculosis and disease
  2. Parents refusing for consent
  3. patient
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
62 participants (actual)
Patient registry
No

Groups and cohorts

  • Mesh infection

    Participants undergoing open Incisional hernioplasty who develop mesh related infection during the postoperative followup period

06

What researchers measure

Primary outcomes

  1. Number and percentage of participants with Mesh related infection following open Incisional hernioplasty

    Development of mesh related infection following open Incisional hernioplasty assessed during postoperative followup will be accessed by clinical examination of the surgical site. The outcome will be measured as the number of participants who developed mesh related infection and percentage of mesh related infection.

    Time frame: 1 month, 3 months and 1 year after surgery

07

Study locations

1 site
  • Dr Faisal Masood teaching Hospital Sargodha
    Sargodha, Punjab Province 40100, Pakistan
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it moved

Ran from Sep 2025 to primary completion in Feb 2026, 5 months.

Since we started tracking on Sep 25, 2026, the dates moved once, on Nov 10, 2026: primary completion Jul 2026 → Feb 2026 and completion Jul 2026 → Feb 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Aug 22, 2026
First posted
Aug 27, 2026
StartActual
Sep 22, 2025
Primary completionActual
Feb 22, 2026was Jul 2026
CompletionActual
Feb 22, 2026was Jul 2026
Last update
Nov 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Primary completion
Jul 25, 2026→Feb 22, 2026
Nov 10, 2026
Study completion
Jul 29, 2026→Feb 22, 2026
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    Primary completion Jul 25, 2026→Feb 22, 2026
    Study completion Jul 29, 2026→Feb 22, 2026
    + 2 other changes: identifiers and verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07790952
Lead sponsor
Sargodha Medical College
Responsible party
Sponsor
First posted
Aug 27, 2026
Start date
Sep 22, 2025
Primary completion
Feb 22, 2026
Completion
Feb 22, 2026
Last update
Nov 10, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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