Anterior Iliac Block for Postoperative Pain and Satisfaction in 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 interventional study evaluates the anterior iliac block as an alternative regional anesthesia technique for patients undergoing inguinal hernia repair with spinal anesthesia. The study compares the block plus standard care to a control group to see if it extends postoperative analgesia duration and enhances patient satisfaction. Eligibility includes adults 18-65 years with ASA I-II status. Exclusions include refusal, contraindications, pregnancy, and higher ASA classes. The trial is conducted at Şanlıurfa Mehmet Akif İnan Training and Research Hospital in Turkey.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 18-65 years patient
* American Society of Anesthesiologists(ASA) I-II patient

Exclusion Criteria:

* Patients who declined to participate in the study
* Patients with contraindications to the anterior iliac block
* Pregnant or breastfeeding patients
* Patients classified as ASA III, IV, or V

Where it's running

• Şanlıurfa Mehmet Akif İnan Training and Research Hospital
  Sanliurfa, Turkey (Türkiye) Recruiting
• Şanlıurfa Mehmet Akif İnan Training and Research Hospital
  Sanliurfa, Turkey (Türkiye) Not yet recruiting

Study contacts

• Principal investigator: Abdullah Şengül, Md — Şanlıurfa Mehmet Akif İnan Training and Research Hospital
• Study coordinator: Abdullah Şengül, Md
• Email: abdullahsengul342@gmail.com
• Phone: +905077345751

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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.