Same Day Discharge for Wedge Resection
The Development of a Novel Same Day Discharge Program After Pulmonary Resection: A Safety and Feasibility Pilot Study
1 other identifier
interventional
54
1 country
1
Brief Summary
Monitoring carefully selected participants to determine if participants can be safely discharged the same day of pulmonary resection
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable surgery
Started Feb 2022
Typical duration for not_applicable surgery
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 24, 2021
CompletedFirst Posted
Study publicly available on registry
October 5, 2021
CompletedStudy Start
First participant enrolled
February 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2024
CompletedMay 31, 2024
May 1, 2024
2 years
September 24, 2021
May 30, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Rate of successful same day discharge
These patients will have their chest tube removed once they meet chest tube removal criteria and will be discharged home once they meet discharge criteria.
2 years
Study Arms (1)
Discharge
OTHERPhase 1-Patients will continue to be admitted after their surgery as is the current practice. Phase 2-Patients will have their chest tube removed once they meet chest tube removal criteria and will be discharged home once they meet discharge criteria.
Interventions
Eligibility Criteria
You may qualify if:
- Patients aged 18 years of age and older who are scheduled to undergo an elective minimally invasive wedge resection of their lung.
You may not qualify if:
- Pulmonary function tests demonstrating forced expiratory volume in 1 second (FEV1) \<50% predicted, FEV1 \<1.5L and/or diffusion lung capacity of carbon monoxide (DLCO) \<50% predicted.
- Patient receives an intraoperative pleurodesis.
- Conversion to open thoracotomy or mini thoracotomy intraoperatively.
- Active pregnancy.
- Thoracic Revised Cardiac Risk Index Score (ThRCRI)8 \>2.
- Underlying cognitive disorder resulting in inability to complete activities of daily living.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
London Health Sciences Centre
London, Ontario, N6A 5W9, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rahul Nayak
Western University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director of Research
Study Record Dates
First Submitted
September 24, 2021
First Posted
October 5, 2021
Study Start
February 1, 2022
Primary Completion
January 15, 2024
Study Completion
March 31, 2024
Last Updated
May 31, 2024
Record last verified: 2024-05
Data Sharing
- IPD Sharing
- Will not share