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Procedure

Robotic Lobectomy for Lung Cancer (OTC-RATS Trial)

N/A
Waitlist Available
Led By Moishe Liberman, MD
Research Sponsored by Centre hospitalier de l'Université de Montréal (CHUM)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 1 year
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing a new way to perform lung surgery using a robot through small cuts below the ribs. It targets patients with early-stage lung cancer who are already scheduled for minimally invasive surgery. The robot helps the surgeon make precise movements, which could reduce pain and speed up recovery. Robotic surgery has been increasingly used in thoracic procedures, offering benefits such as lower blood loss and improved lymph node removal.

Who is the study for?
This trial is for adults with early-stage lung cancer (stage I) who are already scheduled to have a lobectomy, which is surgery to remove a part of the lung, using minimally invasive techniques at CHUM. Pregnant individuals or those unable to consent are not eligible.
What is being tested?
The study is testing the feasibility and safety of performing robotic-assisted thoracic surgery (RATS) lobectomies outside the traditional setting ('Outside the Cage') in patients with stage I lung cancer.
What are the potential side effects?
While specific side effects aren't listed, typical risks may include complications from surgery such as pain, infection, bleeding, and issues related to anesthesia.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 1 year for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
30-day mortality
Conversion rate
Secondary study objectives
Analgesic complementation requirement
Estimated blood loss
Evaluate Chronic Pain
+6 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Out of the Cage Robotic LobectomyExperimental Treatment1 Intervention
Consented patients will undergo lobectomy by OTC RATS following the exact standard steps usually done by VATS/RATS, except for the incisions, that will consist in 1 to 4 subcostal ports, based on the patient and case characteristics.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for lung cancer include surgery, radiation therapy, chemotherapy, targeted therapy, and immunotherapy. Surgery, such as RATS Lobectomy, involves the physical removal of the tumor and is crucial for early-stage lung cancer as it can potentially cure the disease. Radiation therapy uses high-energy rays to kill cancer cells, often used when surgery isn't an option. Chemotherapy involves drugs that kill rapidly dividing cells, including cancer cells, and is used for more advanced stages. Targeted therapy focuses on specific genetic mutations in cancer cells, offering a more personalized treatment with potentially fewer side effects. Immunotherapy boosts the body's immune system to fight cancer. These treatments are vital as they offer multiple approaches to manage and potentially cure lung cancer, improving survival rates and quality of life for patients.
Are three doses of stereotactic ablative radiotherapy (SABR) more effective than 30 doses of conventional radiotherapy?The management of non-small-cell lung cancer: a case history.

Find a Location

Who is running the clinical trial?

Centre hospitalier de l'Université de Montréal (CHUM)Lead Sponsor
377 Previous Clinical Trials
131,280 Total Patients Enrolled
Moishe Liberman, MDPrincipal InvestigatorCentre hospitalier de l'Université de Montréal (CHUM)
3 Previous Clinical Trials
565 Total Patients Enrolled
~0 spots leftby Dec 2024