Predictor of Mesh ConditionNCT07790952
Predictors of Mesh Infection After Open Incisional Hernioplasty
An observational study of Predictor of Mesh Condition, run by Sargodha Medical College at 1 site in Pakistan.
Trial 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 more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Predictor of Mesh Condition
- How many people
- 62 participants
- Where
- 1 sitePakistan
- Study dates
- 22 Sep 2025to 29 Jul 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
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
Who may be able to join
- All age group patient will be included
- Both genders will be involved in this study
- Incisional hernia as per operational definition
Who cannot join
- Co- Morbid condition including hypertension, Tuberculosis and Autoimmune disease
- Parents refusing for consent
- Immunocompromised patient
Trial locations and contacts
1 site in 1 country.
Pakistan1 site
Dr Faisal Masood teaching Hospital Sargodha
Sargodha, Punjab Province, 40100
About this study
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.
- Conditions
- Predictor of Mesh Condition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Mesh infection | Participants undergoing open Incisional hernioplasty who develop mesh related infection during the postoperative followup period |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: 1 month, 3 months and 1 year after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Aug 2026
- Study start22 Sep 2025
- Primary completion25 Jul 2026
- Study completion29 Jul 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Predictor of Mesh ConditionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 62 participants (actual)
Sponsor and investigators
- Lead sponsor
- Sargodha Medical College
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07790952
- Sponsor's protocol ID
- SMC-GS-2026-012
- Status last verified
- Aug 2026
- First submitted
- 22 Aug 2026
- Last updated
- 27 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Predictors of Mesh Infection After Open Incisional Hernioplasty
- ClinicalTrials.gov ID
- NCT07790952
- Acronym / sponsor ID
- SMC-GS-2026-012
- Conditions
- Predictor of Mesh Condition
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 62 participants (actual)
- Lead sponsor
- Sargodha Medical CollegeUniversity, hospital or other
- Study start
- 22 Sep 2025 (actual)
- Primary completion
- 25 Jul 2026 (actual)
- Study completion
- 29 Jul 2026 (actual)
- First posted
- 27 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To determine the frequency of mesh infection in patient with open Incisional hernioplasty and to compare factors contributing with and without mesh infection
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Mesh infection | – | –Participants undergoing open Incisional hernioplasty who develop mesh related infection during the postoperative followup period |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- 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
Key inclusion criteria (3 listed)
- All age group patient will be included
- Both genders will be involved in this study
- Incisional hernia as per operational definition
Key exclusion criteria (3 listed)
- Co- Morbid condition including hypertension, Tuberculosis and Autoimmune disease
- Parents refusing for consent
- Immunocompromised patient
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Number and percentage of participants with Mesh related infection following open Incisional hernioplasty
Time frame: 1 month, 3 months and 1 year after surgery
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Aug 2026.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Predictor of Mesh Condition, run by Sargodha Medical College at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 27 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number and percentage of participants with Mesh related infection following open Incisional hernioplasty (time frame: 1 month, 3 months and 1 year after surgery). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Aug 2026.