CompletedNot Applicable

Dexmedetomidine in TAP Block for Inguinal Hernia Repair

Greece60 participantsStarted 2018-04-01

Plain-language summary

This prospective double-blind randomized study will aim at evaluating the short- and long-term postoperative analgesic efficacy of the ultrasound-guided transversus abdominis plane (TAP) block with a combination of local anesthetic and dexmedetomidine in inguinal hernia repair under general anesthesia

Who can participate

Age range

18 Years – 80 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * American Society of Anesthesiologists (ASA) patients I-III undergoing inguinal hernia repair with a mesh * open hernia repair * elective surgery Exclusion Criteria: * inability to consent to the study due to language barriers or cognitive dysfunction - * bilateral inguinal hernia repair, * body mass index over 40 kg m-2, * skin infection at the puncture site * contraindication to paracetamol or non-steroidal anti-inflammatory drug (NSAIDs) administration * known previous hepatic or renal impairment as assessed by the patients' history and routine biochemical markers * coagulation abnormalities * history of gastroesophageal reflux and preoperative use of opioids or NSAIDs for chronic pain conditions * reoperation of recurrent inguinal hernia after previous mesh repair

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

pain score 3 hours postoperatively

Timeframe: 3 hours after surgery

pain score 6 hours postoperatively

Timeframe: 6 hours after surgery

pain score 24 hours postoperatively

Timeframe: 24 hours after surgery

Trial details

NCT IDNCT04403711

SponsorAretaieion University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12-31

View on ClinicalTrials.gov More Inguinal Hernia trials