The Effect of Preemptive Regional Anesthesia (TAP-block) on Acute and Chronic Pain After Transabdominal Preperitoneal Inguinal Hernia Repair (TAPP)
Unknown statusNot applicableNCT06406959
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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)
The study is devoted to the impact of preemptive regional Transversus abdominal plane block on the postoperative acute and chronic pain after elective Transabdominal preperitoneal (TAPP) inguinal hernia repair.
Study details
- Official title
- The Effect of Preemptive Regional Anesthesia (TAP-block) on Acute and Chronic Pain After Transabdominal Preperitoneal Inguinal Hernia Repair (TAPP) - a Randomized Controlled Trial
- Conditions
- Primary Inguinal Hernia
- Interventions
- Procedure: Transversus abdominal plane block (TAP block)
- Sponsor
- Pirogov Russian National Research Medical University
- Start date
- 2024-03-01
- Primary completion
- 2024-12-31
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Russia
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients with unilateral primary inguinal hernia who are scheduled for elective Transabdominal preperitoneal inguinal hernia repair (TAPP) * Signed Informed consent to participation * ASA I-III * BMI ≤35 kg/m2 Non-inclusion Criteria: * Inguinoscrotal hernia (hernia passing through the entrance to the scrotum) * Previously diagnosed mental disorders * Patients receiving psychotropic drugs and drugs affecting adrenal cortex function (estrogens and systemic glucocorticoids) * Language barrier Exclusion Criteria: * Deviations during the operation/anesthesia that required transfer to the intensive care unit or conversion to open surgery * Refusal to participate
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06406959