Trial · NCT06121726
Predictive Factors for the Effectiveness of the Ilioinguinal Iliohypogastric Nerve Block for Hernia Surgery
NCT06121726, Completed, University of Padova
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Predictive Factors for the Effectiveness of the Ilioinguinal Iliohypogastric Nerve Block for Hernia Surgery. Trials, record NCT06121726. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06121726
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Predictive Factors for the Effectiveness of the Ilioinguinal Iliohypogastric Nerve Block for Hernia Surgery
- NCT number
- NCT06121726
- Status
- Completed
- Enrollment
- 343 participants, actual
- Lead sponsor
- University of Padova
- Conditions
- Hernia Inguinal, Pain Postoperative, Regional Anesthesia
- Interventions
- Ilioinguinal-Iliohypogastric nerve block, Local anesthetic
- First posted
- 2023-11-08
- Last updated
- 2025-05-07
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | ilioinguinal-iliohypogastric nerve block failure | through surgery completation, an average of 1 hour | Described as the need of additional local anesthetic, additional opioids and/or general anesthesia |
| Secondary | Total body weight (kg) as predictive parameter for ilioinguinal-iliohypogastric nerve block failure | through surgery completation, an average of 1 hour | Total body weight (kg) as predictive parameter for ilioinguinal-iliohypogastric nerve block failure |
| Secondary | Time From Block To Skin Incision(minutes) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure | through surgery completation, an average of 1 hour | Time From Block To Skin Incision(minutes) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure |
| Secondary | Dose of anesthetic(mg) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure | through surgery completation, an average of 1 hour | Dose of anesthetic(mg) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure |
| Secondary | Local anesthetic volume(mL) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure | through surgery completation, an average of 1 hour | Local anesthetic volume(mL) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure |
| Secondary | Age(years) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure | through surgery completation, an average of 1 hour | Age(years) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure |
| Secondary | Ultrasound Nerves Visualization (yes/no) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure | through surgery completation, an average of 1 hour | Ultrasound Nerves Visualization (yes/no) As Predictive Parameter For ilioinguinal-iliohypogastric nerve block failure |
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/NCT06121726
GET https://conductscience.org/api/trials/v1/NCT06121726/registered