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Selective Neurectomy and Mesh Removal for Chronic Postherniotomy Pain

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Rigshospitalet

Status

Completed

Conditions

Pain

Study type

Observational

Funder types

Other

Identifiers

NCT00627289
(KF) 11 320499.

Details and patient eligibility

About

Chronic postherniotomy pain affects every day activities in 5-8% of patients. However, no established treatment for this pain syndrome exists and previous reports on the effect of surgical intervention suffer from methodological problems. The neurophysiological characteristics suggest that pain arises from deeper neuronal structures injured during surgery or by ongoing inflammation from the mesh. This study investigates the effect of removing inserted mesh and compressed nerves on pain related daily impairment of activities assessed by the validated AAS questionnaire before and 6 months after surgery

Enrollment

21 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult ( more than 18 years old) patients with chronic pain after groin hernia surgery, and pain related impairment of everyday function. The pain should have occurred after previous open surgery.
  • The patient should be able to locate to a specific area with maximum pain. Patients should be able to understand and use pain scales, and the AAS-scale.

Exclusion criteria

  • All that contradicts the above

Trial design

21 participants in 1 patient group

1
Description:
patients with chronic postherniotomy pain (\>1 year), affecting everyday activities severely

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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