Comparative Study of Inguinodynia After Inguinal Hernia Repair
CompletedNot applicableNCT03678272
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
To evaluate the postoperative pain and the relapse after the repair of the inguinal hernia by Lichtenstein technique with four different mesh types with different types of fixation in patients undergoing major ambulatory surgery.
Study details
- Conditions
- Inguinal Hernia
- Inguinal Hernia Repair
- Open Inguinal Hernia
- Interventions
- Procedure: HERNIOPLASTY WITH PANAVALE MESH
- Procedure: HERNIOPLASTY WITH PARIETEX PROGRIP MESH
- Procedure: HERNIOPLASTY WITH ADHESIX MESH
- Procedure: HERNIOPLASTY WITH TIMESH MESH
- Sponsor
- Hospital General Universitario Elche
- Start date
- 2013-04
- Primary completion
- 2015-03
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Total sites listed
- 0
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Age: over 18 years * Patients undergoing INGUINAL HERNIA surgery on a scheduled basis in surgery without hospitalization. * Sign informed consent. * ASA I-II. * Inguinal hernia. * Unilateral or bilateral hernia. * Lichtenstein hernia repair technique Exclusion Criteria: * Patients with ASA III-IV. * Psychiatric disorders. * Pregnant or breastfeeding. * Non-acceptance of informed consent. * No acceptance or inability to follow a follow-up protocol. * Any hernia repair technique other than Lichtenstein. * Recurrent inguinal hernia
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03678272