Liver Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People whose overall physical health before surgery is rated as either "ASA II" (mild systemic disease) or "ASA III" (serious systemic disease) — a classification assigned by an anaesthesiologist (confirm with trial site)
- People with a Body Mass Index (BMI) between 20 and 35 kg/m²
Who may not be able to join:
- People who do not wish to participate
- People whose pre-surgery health is rated as "ASA IV" (severe, life-threatening systemic disease) by an anaesthesiologist
- People with a BMI below 20 or above 35 kg/m²
- People with a known allergy, sensitivity, or medical reason to avoid the study medications, which include local anaesthetics and opioid pain relievers
- People with a history of psychological disorders and/or chronic pain
- People for whom nerve-blocking anaesthesia techniques are not safe, such as those with a local skin infection, pre-existing nerve damage, or blood clotting problems
- People with severe heart, breathing, or kidney disease
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: sayed M Abed, Cairo University
Phone: 1226806532
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
post-operative analgesic consumption for 24 hours among study groups.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.