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Neurophysiological Characterization of Postherniotomy Pain

Quantitative Sensory Testing in Persistent Postherniotomy Pain Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00719368
Enrollment
48
Registered
2008-07-21
Start date
2006-01-31
Completion date
2012-09-30
Last updated
2014-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuropathic Pain, Postherniotomy Pain, Postoperative Pain

Keywords

Groin hernia, pain, chronic, quantitative sensory testing, Persistent postoperative pain

Brief summary

Sensory function is different in persistent postherniotomy pain patients than in operated controls, suggesting this to be a neuropathic pain syndrome. By performing quantitative sensory testing, the specific changes in pain patients will be revealed, thereby aiding in designing future treatment trials. MRI scans of the groin regions in pain patients and control patients will be evaluated by senior MRI specialists assessing potential pathology to the region (Mesh, inflammation, edema, funicle etc.) Assessors will be blinded to clinical status, and surgery.

Interventions

None listed

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Observational model
COHORT

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Male patients \>18 yrs * Inguinal herniotomy \>1 yr previously * No sign of hernia recurrence * Unilateral chronic groin pain lasting more than 3 months * Moderate/severe pain related impairment of everyday activities.

Exclusion criteria

* Other causes of persistent pain in groin region (hip, other surgical procedures)

Design outcomes

Primary

MeasureTime frame
Sensory functionactual

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026