Trial · NCT07896278
Onlay vs. Sublay Mesh Hernioplasty for Primary Ventral Hernia
NCT07896278, Not applicable, Completed, Provincial Headquarter Teaching Hospital Gilgit
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Onlay vs. Sublay Mesh Hernioplasty for Primary Ventral Hernia. Trials, record NCT07896278. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896278
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Onlay vs. Sublay Mesh Hernioplasty for Primary Ventral Hernia
- NCT number
- NCT07896278
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 76 participants, actual
- Lead sponsor
- Provincial Headquarter Teaching Hospital Gilgit
- Conditions
- Ventral Hernia Repair, Hernia Abdominal Wall
- Interventions
- Onlay Mesh Hernioplasty, Sublay Mesh Hernioplasty
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postoperative Pain | 12 hours, 4 days. 2 weeks | Pain intensity will be measured using a Visual Analogue Scale (VAS) from 0 (no pain) to 10 (worst pain). |
| Primary | Seroma Formation | Seroma will be assessed at the 7th and 14th postoperative days, and during follow-up up to 6 months. | Accumulation of clear, serous fluid at the surgical site will be confirmed by clinical examination or ultrasonography (anechoic/hypoechoic fluid collection). |
| Primary | Hematoma Formation | Hematoma will be assessed at the 7th and 14th postoperative days, and during follow-up up to 6 months. | Accumulation of blood at the surgical site will be confirmed by clinical examination (bruising, tender swelling) or ultrasonography (complex fluid collection). |
| Primary | Wound Infection | Wound infection will be assessed at the 7th and 14th postoperative days, and during follow-up up to 6 months. | Microbial contamination at the surgical site will be characterized by signs of inflammation (hyperemic, painful, hot swelling) with or without purulent discharge, requiring intervention. |
| Primary | Recurrence of Hernia | 6 months | Return of the hernia at the surgical site will be confirmed through clinical and sonological findings. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07896278
GET https://conductscience.org/api/trials/v1/NCT07896278/registered