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Clinical Trials/ISRCTN20639281
ISRCTN20639281
Completed
未知

A randomized clinical trial to assess the efficacy of patient-controlled paravertebral block versus thoracic epidural analgesia for patients undergoing single intercostal video-assisted thoracic surgery

Second Affiliated Hospital of Zhejiang University0 sites176 target enrollmentJanuary 23, 2020
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ConditionsPain in the postoperative periodSurgery

Overview

Phase
未知
Intervention
Not specified
Conditions
Pain in the postoperative period
Sponsor
Second Affiliated Hospital of Zhejiang University
Enrollment
176
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37573993/ (added 06/06/2024)

Registry
who.int
Start Date
January 23, 2020
End Date
July 31, 2022
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Second Affiliated Hospital of Zhejiang University

Eligibility Criteria

Inclusion Criteria

  • •Patients diagnosed with solitary pulmonary nodules and without chronic pain (with no pain medications routinely used) deemed suitable to undergo three\-port single\-intercostal VATS by surgeons

Exclusion Criteria

  • •Patients with other malignancies

Outcomes

Primary Outcomes

Not specified

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