Surgical Outcomes Following Neurectomy Based Upon Response to Local Anesthetic Injection in Chronic Groin Pain
NCT ID: NCT05386693
Last Updated: 2024-04-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
10 participants
OBSERVATIONAL
2022-04-20
2024-03-25
Brief Summary
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Detailed Description
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Specific Aims
During the preoperative assessment for neurectomy, patients undergo a minor procedure involving injecting a local analgesic around the nerve, a nerve block. In this study, the investigators propose providing the patients with pain and quality of life questionnaires and tools to assess their baseline pain, response to the local analgesics, and response to the neurectomy procedure. The specific aims of the study are:
1. Evaluate the reliability of nerve block to predict patient response to neurectomy procedure:
While nerve blocks have been frequently used as part of the preoperative assessment to neurectomy, the response from nerve block has not been correlated with post-neurectomy pain outcomes. The investigators intend to objectively assess pain relief in response to nerve block and neurectomy in this specific aim.
The investigators hypothesized that patients who reported relief in response to nerve blocks would have pain relief from post neurectomy procedure, and patients who did not experience relief from nerve blocks will not have relief from post neurectomy procedure.
2. Evaluate the correlation between the extent of pain relief from nerve block to post neurectomy pain relief:
The Visual Assessment Scale (VAS) is a tool that provides a quantified assessment of pain. Assessing the pain with VAS before and after nerve block will provide a scale of change in pain level in response to the nerve block injection, the extent of which can be correlated with post neurectomy VAS to predict the outcome. The investigators hypothesize that patients with a greater improvement in pain level in response to nerve block have a higher chance of achieving pain relief with neurectomy than those with a low improvement in pain level from the nerve block.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Ilioinguinal Nerve Block
Ilioinguinal nerve block
Local anesthetic injection of the ilioinguinal nerve. This is performed in the outpatient clinic.
Interventions
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Ilioinguinal nerve block
Local anesthetic injection of the ilioinguinal nerve. This is performed in the outpatient clinic.
Eligibility Criteria
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Inclusion Criteria
* Chronic groin pain
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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The Cleveland Clinic
OTHER
Responsible Party
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David Krpata
Principal Investigator
Locations
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Cleveland Clinic
Cleveland, Ohio, United States
Countries
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Other Identifiers
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21-1176
Identifier Type: -
Identifier Source: org_study_id
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