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Bilateral Superficial Cervical Plexus Block in Thyroid/Parathyroid Surgery

NCT04051099 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2021-05-24

No results posted yet for this study

Summary

To compare efficacy and safety between bilateral superficial cervical plexus block combined with intravenous sedation (RA group) and general anesthesia (GA group) for thyroid and parathyroid operations. This study evaluates postoperative numerical pain score and systemic opioid requirement within 24 hours.

Conditions

  • Benign Tumor of Thyroid
  • Hyperparathyroidism

Interventions

PROCEDURE

Bilateral superficial cervical plexus block with 0.25% bupivacaine 8 ml each (total 16 ml)

bilateral superficial cervical plexus

DRUG

Dexmedetomidine plus propofol infusion

Dexmedetomidine 0.5 ug/kg infusion in 10 min then 0.5 ug/kg/h, Propofol infusion

PROCEDURE

Local infiltraion analgesia

local infiltration analgesia with 2%lidocaine with adrenaline 5 ug/ml 10 ml

PROCEDURE

General anesthesia with endotracheal tube

Induction with Propofol and intubation with cisatracurium

Sponsors & Collaborators

  • Mahidol University

    lead OTHER

Principal Investigators

  • Suwimon Tangwiwat, MD · Siriraj Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-01
Primary Completion
2021-09-30
Completion
2021-12-15

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04051099 on ClinicalTrials.gov