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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 December 2017 |
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Main ID: |
NCT03242668 |
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Date of registration:
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25/07/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Paravertebral Block for Postoperative Analgesia in Thoracoscopic Surgery
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Scientific title:
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Patient Controlled Paravertebral Analgesia for Video-assisted Thoracoscopic Surgery |
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Date of first enrolment:
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June 1, 2016 |
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Target sample size:
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30 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03242668 |
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Study type:
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Interventional |
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Study design:
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Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Vietnam
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- American Society of Anesthesiologists class I to III risk undergoing elective VATS,
aged 32-72 years, scheduled for lung resection surgery.
Exclusion Criteria:
- Patients who refused to participate, less than 18 years of age, ASA physical status 3
or more,, allergy to any of the study drugs, patients having any contraindication to
placement of PVB, kyphoscoliosis, presence of acute herpes zoster, chronic pain
syndrome, chronic analgesic use and psychiatric disease.
Age minimum:
20 Years
Age maximum:
75 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Pain, Postoperative
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Intervention(s)
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Drug: PCA
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Procedure: PVB using PVC
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Procedure: VATS
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Primary Outcome(s)
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VAS score at rest and on coughing
[Time Frame: 72 hours]
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Secondary Outcome(s)
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Analgesia effects on respiratory function
[Time Frame: three postoperative consecutive days]
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Patient's satisfaction
[Time Frame: three postoperative consecutive days]
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Rescue analgesia
[Time Frame: three postoperative consecutive days]
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The number dermatome inhibition
[Time Frame: three postoperative consecutive days]
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Arterial blood gas values
[Time Frame: three postoperative consecutive days]
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Secondary ID(s)
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103HospitalVMMU
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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