Same Day Discharge for Video-Assisted Thoracoscopic Surgery (VATS) Lung Surgery

Trial Title: Same Day Discharge for Video-Assisted Thoracoscopic Surgery (VATS) Lung Surgery

NCT ID: NCT05583916

Condition: Lung Cancer
Surgery

Conditions: Keywords:
Same Day Discharge
Video-Assisted Thoracoscopic Surgery (VATS)
Minimally Invasive Surgery
Enhanced Recovery Pathway

Study type: Interventional

Study phase: N/A

Overall status: Unknown status

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Procedure
Intervention name: Same Day Discharge - Video-Assisted Thoracoscopic Surgery (VATS) Lung
Description: All patients will be scheduled to surgery at the start of the day and will be discharged within the same day as the procedure.
Arm group label: Lung Cancer Patients

Summary: Phase I to evaluate the safety and feasibility of same-day discharge in selected participants undergoing minimally-invasive lung surgery and who receive an enhanced recovery pathway.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Signed or verbal informed consent by participant - Male and female adults, age 18 and above - Clinical stage I-II lung cancer (suspected, proven, unproven), or secondary pulmonary malignancy - BMI < 35 - ECOG 0-1 - Eligible for surgery and lung cancer resection (FEV1 > 60%, DLCO > 60%) - Elective VATS anatomic resection (segmentectomy or lobectomy), or wedge resection - Capable caregiver for discharge home Exclusion Criteria: - Clinical stage III lung cancer - Surgery requiring pneumonectomy - Neoadjuvant therapy - Active pregnancy or breastfeeding - History of chronic pain syndromes - History of chronic opioid use - Concomitant major surgery indicated with current admission to hospital - Anticipated intraoperative complication including conversion to thoracotomy, major bleeding requiring blood transfusion, extensive adhesiolysis, injury to mediastinal structures, airway injury, nerve injury (phrenic, recurrent) - Need for epidural or patient-controlled intravenous analgesia - Need for urinary catheter

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: McGill University Health Centre

Address:
City: Montreal
Zip: H4A 3J1
Country: Canada

Status: Recruiting

Contact:
Last name: Jonathan Spicer, MD PhD

Start date: September 7, 2022

Completion date: October 2023

Lead sponsor:
Agency: McGill University Health Centre/Research Institute of the McGill University Health Centre
Agency class: Other

Source: McGill University Health Centre/Research Institute of the McGill University Health Centre

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05583916