Prolonged Hospital Stay After Thoracoscopic Anatomical Lung Resections
NCT ID: NCT06638645
Last Updated: 2025-01-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
140 participants
OBSERVATIONAL
2024-11-12
2025-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients undergoing a minimally invasive anatomical lung resection
Patients undergoing a minimally invasive anatomical lung resection, receiving perioperative care according to the ERAS protocol for Lung Surgery
VATS/RATS anatomical lung resection
Perioperative care according to the ERAS protocol for lung surgery
Interventions
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VATS/RATS anatomical lung resection
Perioperative care according to the ERAS protocol for lung surgery
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Informed consent obtained pre-operatively
* Age 18 years or older
Exclusion Criteria
* Traumatic event as indication for lung resection
* Non-anatomical lung resections
* Thoracotomy
* Patients already hospitalized for other pathologies, pre-existent and not related to the lung surgery
* Urgent/emergency procedures
18 Years
ALL
No
Sponsors
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AZ Sint-Lucas Brugge
OTHER
University Hospital, Ghent
OTHER
Responsible Party
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DienstThoracaleEnVasculaireHeelkunde
Clinical professor
Locations
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AZ Sint-Jan Brugge-Oostende AV
Bruges, , Belgium
Ghent University Hospital
Ghent, , Belgium
Countries
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Central Contacts
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Facility Contacts
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Jan Lesaffer, MD
Role: backup
Lauren Villeirs, MD
Role: backup
Liesbeth Desender, MD, PhD
Role: backup
Other Identifiers
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THE-2024-0246
Identifier Type: -
Identifier Source: org_study_id
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