Postoperative Analgesia y After Uniportal Video-assisted Thoracoscopic Surgery
NCT ID: NCT05242328
Last Updated: 2023-02-27
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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UNKNOWN
NA
40 participants
INTERVENTIONAL
2021-01-05
2024-12-26
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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post-operative VAS score of Ultrasound-guided erector spinae plane block
Ultrasound-guided erector spinae plane block
Ultrasound-guided erector spinae plane block
post-operative VAS score of surgical thoracoscopic intercostal nerve block
surgical thoracoscopic intercostal nerve block
surgical thoracoscopic intercostal nerve block
Interventions
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Ultrasound-guided erector spinae plane block
Ultrasound-guided erector spinae plane block
surgical thoracoscopic intercostal nerve block
surgical thoracoscopic intercostal nerve block
Eligibility Criteria
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Inclusion Criteria
* undergoing elective uniportal VATS lobectomy.
Exclusion Criteria
* body mass index \> 35 kg/m2,
* American society of anesthesiologists (ASA) grade above 3,
* contraindication to nerve block,
* allergy to analgesic agents,
* regular opioid used for chronic pain prior to this time surgery,
* conversion to thoracotomy or VATS procedure,
* postoperative intubation,
* postoperative intensive care unit admission.
20 Years
ALL
No
Sponsors
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National Cheng-Kung University Hospital
OTHER
Responsible Party
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Principal Investigators
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Shuoying Dai
Role: STUDY_CHAIR
National Cheng-Kung University Hospital
Locations
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National Cheng Kung University Hospital
Tainan City, , Taiwan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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A-ER-110-293
Identifier Type: -
Identifier Source: org_study_id
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