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NCT04773509 Clinical Trial

Effect of Intraoperative Paravertebral Block on Postoperative Pain and Recovery in Patients Undergoing Mechanical Correction for Scoliosis

Scoliosis Clinical Trial

Official title:
Effect of Intraoperative Paravertebral Block on Postoperative Pain and Recovery in Patients Undergoing Mechanical Correction for Scoliosis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04773509
Other study ID # 4-2020-1467
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 24, 2021
Est. completion date December 24, 2023

Study information
Verified date July 2021
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pain management after scoliosis surgery is challenging for the anesthesiologists. This surgery causes severe postoperative pain and patients undergoing these operations are children or adolescents who are increased pain sensation compared with adults. Therefore, we aim to evaluate whether intraoperative paravertebral block (PVB) decreases postoperative pain in these patients. Thirty-two patients scheduled for mechanical correction due to scoliosis will be divided into PVB (n=16) and control (n=16) groups. Randomly selected patients of the PVB group are performed PVB with 0.2% ropivacaine on both sides. In contrast, PVB are not performed in the control group.

Recruitment information / eligibility
Status Completed
Enrollment 32
Est. completion date December 24, 2023
Est. primary completion date December 24, 2023
Accepts healthy volunteers No
Gender All
Age group 10 Years to 18 Years
Eligibility Inclusion Criteria: - Patients undergoing mechanical correction Exclusion Criteria: - The subjects who cannot communicate - The subject is a foreigner or illiterate

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Paravertebral block
Randomly selected patients of the PVB group are performed PVB with 0.2% ropivacaine on both sides.

Locations
Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Severance Hospital, Yonsei University College of Medicine Seoul

Sponsors (1)
Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain score visual analog scale (VAS) (0-10) 6 hours after the end of surgery
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