Trial · NCT07909148
Parastomal Hernia at 1 and 3 Years: Radiological Incidence, Progression, and Impact on Quality of Life
NCT07909148, Recruiting, Region Skane
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Parastomal Hernia at 1 and 3 Years: Radiological Incidence, Progression, and Impact on Quality of Life. Trials, record NCT07909148. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07909148
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Parastomal Hernia at 1 and 3 Years: Radiological Incidence, Progression, and Impact on Quality of Life
- NCT number
- NCT07909148
- Status
- Recruiting
- Enrollment
- 135 participants, estimated
- Lead sponsor
- Region Skane
- Conditions
- Parastomal Hernia, Colorectal Cancer (Diagnosis)
- Interventions
- Routine Surveillance Computed Tomography (CT)
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mean Difference in Total Colostomy Impact Score (CIS) at 3 Years | 3 years post-surgery | The mean difference in total Colostomy Impact Score (CIS) between patients with and without a radiologically confirmed parastomal hernia at the 3-year follow-up. The CIS is a validated questionnaire with a total score ranging from 0 to 38, where higher scores indicate worse quality of life/greater symptom burden (scores 0-9: minor impact, 10-38: major impact). |
| Secondary | Mean Difference in Total Colostomy Impact Score (CIS) at 1 Year | 1 year post-surgery | The mean difference in total Colostomy Impact Score (CIS) between patients with and without a radiologically confirmed parastomal hernia at the 1-year follow-up. |
| Secondary | Mean Difference in EQ-5D-5L Index Values at 1 Year | 1 year post-surgery | The mean difference in EQ-5D-5L index values between patients with and without a radiologically confirmed parastomal hernia at the 1-year follow-up. The index score ranges from 0 (representing death) to 1 (representing full health), with negative values for states worse than death; higher scores indicate better health-related quality of life. |
| Secondary | Longitudinal Change in Generic Quality of Life (EQ-5D-5L Index) | From 1 year to 3 years post-surgery | The longitudinal change in the EQ-5D-5L index value for the total cohort between the 1-year and 3-year follow-ups. The score ranges from 0 to 1, where higher scores indicate better health-related quality of life. |
| Secondary | Incidence of Parastomal Hernia on CT Scans | 1 year and 3 years post-surgery | The incidence of parastomal hernia at 1 and 3 years post-stoma creation, diagnosed by standardized review of routine oncological follow-up CT scans. |
| Secondary | Rate of Radiological Parastomal Hernia Progression | From 1 year to 3 years post-surgery | The rate of hernia progression between the 1-year and 3-year follow-ups, defined by new hernia development, increase in fascial defect size, or change in European Hernia Society (EHS) classification. |
| Secondary | Diagnostic Correlation Between Patient-Reported Suspicion and Radiological Hernia | 1 year post-surgery | The correlation between patient-reported suspicion of a hernia and radiologically confirmed parastomal hernia at the 1-year follow-up. |
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/NCT07909148
GET https://conductscience.org/api/trials/v1/NCT07909148/registered