Trial · NCT07881354
Duramesh Versus Minimally Invasive IPOM for High-Risk Umbilical Hernia Repairs
NCT07881354, Not applicable, Recruiting, Northwestern University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Duramesh Versus Minimally Invasive IPOM for High-Risk Umbilical Hernia Repairs. Trials, record NCT07881354. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07881354
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Duramesh Versus Minimally Invasive IPOM for High-Risk Umbilical Hernia Repairs
- NCT number
- NCT07881354
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 160 participants, estimated
- Lead sponsor
- Northwestern University
- Conditions
- Umbilical Hernia, Ventral Hernia
- Interventions
- Duramesh, Mesh
- First posted
- 2026-10-19
- Last updated
- 2026-11-06
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postoperative Day 1 Pain | Postoperative Day 1 | Pain on the Numeric Rating Scale (0 = no pain, 10 = worst pain imaginable), collected by phone. |
| Secondary | Postoperative pain on day of surgery | Post-anesthesia care unit, day of surgery | Pain intensity measured with the Numeric Rating Scale (NRS) for pain, scored from 0 (no pain) to 10 (worst pain imaginable). Higher scores indicate worse pain. |
| Secondary | Postoperative Day 7 Pain | Postoperative day 7 | Pain intensity measured with the Numeric Rating Scale (NRS) for pain, scored from 0 (no pain) to 10 (worst pain imaginable). Higher scores indicate worse pain. |
| Secondary | Wound complications | 30 days, 1 year and 2 year | seroma, suture sinus, and mesh-related complications |
| Secondary | Hospital readmissions | 30 day, 1 year, 2 year | Hospital readmissions following surgery |
| Secondary | Reoperations | 30 day, 1 year, 2 year | Events where reoperation is done for the hernia |
| Secondary | Return to Normal Activity | 30 days | Number of patients reporting a full return to preoperative daily activities |
| Secondary | Hernia Recurrence | 1 and 2 years | Recurrence by consensus definition (clinical exam, CT imaging, and Ventral Hernia Recurrence Inventory survey) |
| Secondary | Hospital Admission After Surgery | Postoperative day zero, index hospitalization | Proportion of patients requiring admission instead of same-day discharge, and time in recovery before discharge |
| Secondary | Costs | Baseline through hospital discharge, average 5 days | OR direct costs; hospital direct costs; procedural costs |
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/NCT07881354
GET https://conductscience.org/api/trials/v1/NCT07881354/registered