New pain management technique for inguinal hernia surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the effectiveness of the quadro-iliac plane block for managing postoperative pain in patients undergoing elective unilateral laparoscopic inguinal hernia repair. The study compares this novel regional anesthesia technique to standard pain management approaches, which often rely on opioids and nonsteroidal anti-inflammatory drugs. By utilizing a specific fascial plane block, the trial aims to improve pain control and facilitate quicker recovery and discharge for patients. The study will enroll patients aged 18-65 who are undergoing this common surgical procedure under general anesthesia.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients aged 18-65 years
* Undergoing elective,
* unilateral laparoscopic inguinal hernia repair
* Receiving general anesthesia

Exclusion Criteria:

* Patients who refuse to provide consent
* Patients with contraindications to regional anesthesia
* Patients with impaired consciousness
* Patients with coagulopathy
* Patients with infections at the block site
* Emergency cases

Where it's running

• Konya City Hospital
  Konya, Turkey (Türkiye) Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.