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NCT05180214 Clinical Trial

Analgesia for Thyroidectomy Using Bilateral Superficial Cervical Plexus Block With Bupivacaine Only or Adding Ketorolac to it.

Thyroid Nodule Clinical Trial

Official title:
The Effect of Adding Ketorolac to Bupivacaine in Superficial Cervical Plexus Block in Thyroid Surgery.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05180214
Other study ID # 2006
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date January 17, 2021
Est. completion date September 15, 2021

Study information
Verified date January 2022
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thyroidectomy is considered a common operation with moderate to severe postoperative pain in some patients. Patients are divided into two groups. Bupivacaine group received bilateral superficial cervical plexus block (BSCPB) with 10 ml of bupivacaine (0.25%) and 1 ml of normal saline on each side and the Bupivacaine Ketorolac group received (BSCPB) with 10 ml of bupivacaine (0.25%) and 1 ml of ketorolac (15 mg) on each side.

Recruitment information / eligibility
Status Completed
Enrollment 46
Est. completion date September 15, 2021
Est. primary completion date August 19, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Patients aged 20-50 years - ASA I-II patients - Patients going to do thyroid surgeries under general anesthesia Exclusion Criteria: - Patient refusal - Known history of sensitivity to the drug used in the study - Drug abuse - Infection at the site of the block - Presence of coagulopathy

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Bupivacain
analgesic
• Ketorolac
analgesia

Locations
Country Name City State
Egypt Sohag University Faculty of Medicine Sohag

Sponsors (1)
Lead Sponsor Collaborator
Sohag University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary 1st analgesic requirement The first time of supplemental analgesic need postoperatively 24 hours
Secondary analgesic consumption total analgesic consumption 24 hours
Secondary postoperative pain visual analogue scale(0-10) 0=no pain and 10=severe intolerable pain 24 hours
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