Clinical trial Recruiting at 1 site Observational Ages 18 and up

Reducing long-term pain after lung resection using transthoracic, out-of-cage, or hybrid robotic approaches

Official title: Chronic Pain After Thoracic Surgery: Towards a New Standard? A Comparative Prospective Study of Pain Reduction After Pulmonary Resection by RATS-TT, RATS-OTC, and Hybrid RATS.

Run by Centre hospitalier de l'Université de Montréal (CHUM) · NCT07184463 · Data updated 2026-11-12

We will test whether using subcostal/subxiphoid ('out of cage') or a hybrid robotic approach causes less chronic pain than standard transthoracic robotic surgery in adults having lung resection.

More Thoracic Surgery trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment120 (estimated)
SponsorCentre hospitalier de l'Université de Montréal (CHUM)
Academic / other
Locations1 site (Montreal, Quebec)
StatusRecruiting
StartedDecember 5, 2025
Main results expectedJune 2027
Study endsJune 2027
Registry record updatedFebruary 23, 2026
Trial IDNCT07184463 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adult patients (18+) with ASA 1–3 undergoing robotic pulmonary resection at CHUM who can provide consent and complete postoperative pain assessments are ideal candidates.

Probably not a fit

Patients with language, psychiatric, cognitive, or physical barriers to pain assessment, those who refuse participation, or those who require reoperation by VATS or thoracotomy postoperatively are unlikely to benefit from participation.

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

What this trial studies

This observational study compares chronic pain outcomes at 3 and 6 months after pulmonary resection performed with three robotic approaches: transthoracic RATS (RATS-TT), out-of-cage RATS (RATS-OTC), and a hybrid RATS technique. The rationale is that intercostal trocars used in transthoracic approaches can injure intercostal nerves and lead to chronic pain, while subcostal/subxiphoid ports avoid the intercostal space. Patients aged 18 and older with ASA scores 1–3 who undergo robotic pulmonary resection at CHUM will be followed and asked to complete standardized pain assessments. The study will compare the frequency and severity of chronic pain and related opioid use across the three technique groups.

Why it matters

Potential benefit: If successful, the work could identify surgical approaches that reduce the risk of chronic post-thoracic surgery pain and lower long-term opioid needs after lung resection.

How similar studies have gone: A French team reported reduced opioid use and lower acute postoperative pain with the RATS-OTC approach, but chronic pain outcomes have not yet been established in larger or comparative cohorts.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients aged 18 years and older
* American Society of Anesthesiologists (ASA) score 1-3

Exclusion Criteria:

* Language barrier, psychiatric, physical or mental condition making pain assessment impossible despite prior education
* Patient refusal to participate
* Patients reoperated by VATS or thoracotomy in the postoperative period in the context of the occurrence of complications

Where it's running

  • Centre Hospitalier de l'Université de Montreal
    Montreal, Quebec, Canada
    Recruiting

Study contacts

Similar studies

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

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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.