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NCT05386693 · ClinicalTrials.gov registry record

Surgical Outcomes Following Neurectomy Based Upon Response to Local Anesthetic Injection in Chronic Groin Pain

A clinical trial, sponsored by The Cleveland Clinic.

Terminated
Registry status
10
Enrollment target

NCT05386693: Clinical Trial study, sponsored by The Cleveland Clinic.

NCT05386693 is a clinical trial that was terminated before completion, run by The Cleveland Clinic. The registered enrollment target is 10 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05386693 was terminated before completion, sponsored by The Cleveland Clinic.

TERMINATED
Registry status
10 participants
Enrollment target

Study Summary

The management of chronic pain after inguinal hernia surgery presents unique challenges. Ilioinguinal nerve blocks are often used in the initial treatment of this disease. This can often be followed by surgery, including neurectomy and/or hernia mesh removal. In an effort to identify preoperative predictors of postoperative outcomes following these surgical interventions the investigators devised a study to prospectively evaluate and correlate a patients pre-operative response to an ilioinguinal nerve block with their post-operative outcomes following surgery for chronic groin pain after inguinal hernia surgery.

Primary Outcome

Pain as measured with the Visual Analogue Scale (VAS) using a scale of 0 to 100; with 0 being the least amount of pain and 100 being the most amount of pain.

Interventions

  • PROCEDURE Ilioinguinal nerve block

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2022-04-20
Est. Completion 2024-03-25
The Cleveland Clinic

688 total trials

Why NCT05386693 stopped before completion

NCT05386693 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 10 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Ilioinguinal nerve block is the first listed.

NCT05386693 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05386693 about?

NCT05386693 is a clinical study titled "Surgical Outcomes Following Neurectomy Based Upon Response to Local Anesthetic Injection in Chronic Groin Pain". The management of chronic pain after inguinal hernia surgery presents unique challenges. Ilioinguinal nerve blocks are often used in the initial treatment of this disease. This can often be followed by surgery, including neurectomy and/or hernia mesh removal. In an effort to identify preoperative pr...

What is the current status of trial NCT05386693?

This trial is currently terminated. The enrollment target is 10 participants. The study started on 2022-04-20. Estimated completion is 2024-03-25.

What interventions are being tested in trial NCT05386693?

The interventions under investigation include: Ilioinguinal nerve block (PROCEDURE).

Who is sponsoring clinical trial NCT05386693?

This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT05386693, the US trial registry maintained by the National Library of Medicine. NCT05386693 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.