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NCT03731468 Clinical Trial

Ultrasound Guided Intermediate Cervical Plexus Block in Thyroid Surgery

Postoperative Pain Clinical Trial

Official title:
Effect of Dexmethasone Addition to Bupivacaine in Bilateral Intermediate Cervical Block in Thyroid Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03731468
Other study ID # UDLC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 15, 2018
Est. completion date December 1, 2020

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

Clinical Trial Summary

studying the effect of dexmeditomidine addition to bupivacaine in bilateral intermediate cervical block for patients undergoing thyroidectomy under general anaesthesia

Description:

80 patients who will be undergoing elective thyroidectomy will be randomly allocated into one of two groups ; group A will receive 20 mg isobaric bupivacaine + 8 mg dexamethasone(diluted in 5 ml) group B will receive 20 mg isobaric bupivacaine + 1 ml normal saline. block will be done under complete a septic condition after induction of general anaesthesia.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date December 1, 2020
Est. primary completion date January 1, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - Elective surgery - ASA 1, II, AND III Exclusion Criteria: - Patient refusal - Infection at the entry site - BMI > 3

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• local anesthetic
ultrasound guided superficial cervical block in thyroid surgery
• Dexamethasone
dexamethasone will be added to ultrasound guided superficial cervical block in thyroid surgery

Locations
Country Name City State
Egypt Assiut university Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative analgesia duration time of first analgesic requirement is the time of end of block analgesia 24 hour postoperative
Secondary postoperative complications related to the block occurrence of complications secondary to the block well be recorded 8 hours
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