Lung 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 who are scheduled for a planned (non-emergency), single-side lung surgery performed using a small camera and instruments through small cuts in the chest (a type of surgery called VATS)
- People aged between 18 and 80 years old
- People whose general health before surgery falls within a low-to-moderate risk category as assessed by an anaesthesiologist (confirm with trial site)
Who may not be able to join:
- People for whom local numbing medications (local anaesthetics) are not safe to use — for example, due to a skin infection at the injection area, an allergy to these medications, or a blood clotting problem or other bleeding risk
- People who have unusual or altered feeling or sensation in the chest wall area where surgery is planned
- People with liver problems or kidney problems, as measured by specific blood test results being outside certain ranges (confirm exact values with trial site)
- People who are pregnant, breastfeeding, planning to become pregnant during the study period, or people who could become pregnant and are not using a reliable form of contraception
- People who have been using opioid pain medicines before surgery, have a history of long-term (chronic) pain, or have a history of opioid misuse
- People who do not wish to give their formal agreement (informed consent) to take part
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: Xin Y Lv, PhD, Shanghai Pulmonary Hospital, Tongji University, Shanghai, China
Phone: 8615601680288
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
Pain score area under the curve (AUC) from 25 to 72 hours postoperatively
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.