Two nerve-block options for pain control after inguinal hernia repair

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

Adults (18–65) with ASA I–II undergoing elective inguinal hernia repair at Harran University will receive either an anterior iliac block or an ilioinguinal/iliohypogastric block for postoperative analgesia. Investigators will record numeric rating pain scores, duration of analgesia, postoperative analgesic consumption, and patient satisfaction to compare effectiveness. The anterior iliac block is proposed to provide broader dermatomal coverage and potentially longer or more complete analgesia than the conventional ilioinguinal/iliohypogastric block. Safety and block-related adverse events will also be monitored during the postoperative period.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* It includes patients aged 18-65 years
* Classified as ASA I-II
* Who are undergoing elective inguinal hernia surgery

Exclusion Criteria:

* Patients who did not wish to participate voluntarily
* Those with contraindications to the anterior iliac block or the Ilioinguinal/Iliohypogastric block,
* Pregnant or breastfeeding women
* Patients classified as ASA III-IV-V

Where it's running

• Harran University
  Şanliurfa, Hali̇li̇ye, Turkey (Türkiye) Recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Predictors of severe pain within 24 hours after cesarean delivery with spinal anesthesia

  This study will look at which pre-, intra-, and post-operative factors are linked to severe pain in the first 24 hours after an elective cesarean done with spinal anesthesia.

  Recruiting Bursa City Hospital · Bursa, Nilüfer · NCT07789301

• Transverse vs Longitudinal Serratus Anterior Plane Block for Breast Surgery

  This trial tests whether a longitudinal ultrasound view for serratus anterior plane block provides better pain relief after breast surgery than the standard transverse view.

  Recruiting Ankara Etlik City Hospital · Ankara, Yenimahalle\Ankara · NCT07739277

• Combined PECS II and PIP blocks vs TPVB for post-mastectomy pain relief

  This trial tests whether a combination of PECS II and superficial PIP blocks can provide better or similar pain relief after mastectomy compared with the standard thoracic paravertebral block.

  Recruiting Dharmais National Cancer Center Hospital · Jakarta, DKI Jakarta · NCT07738770

• Ketamine or Dexmedetomidine as an Additive to Scalp Block for Brain Tumor Surgery

  This trial tests whether adding ketamine or dexmedetomidine to bupivacaine for scalp blocks improves pain control after supratentorial brain tumor removal.

  Recruiting at 2 sites Cairo University · Cairo, Governorate and 1 other locations · NCT07698665

• Rhythmic Skin Tapping and Internal Vibration for Pediatric Venipuncture Pain and Fear

  This study tests whether light fingertip tapping above the needle site or a humming sound can reduce pain and fear in children aged 6-12 during blood draws.

  Recruiting Akdeniz University · Antalya, Kepez · NCT07650591

• Brief audio-guided mindfulness for pain in orthopedic waiting rooms

  This trial tests whether listening to short mindfulness audio clips can help reduce pain for adults waiting for orthopedic care.

  Recruiting Florida State University · Tallahassee, Florida · NCT07562412

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.