Cervical Block in Thyroid Surgery

Status Completed

Clinical Trial Summary

The study investigates the impact on post-operative pain of the superficial cervical block with bupivacaine combined with subcutaneous infiltration of the incisional area in thyroid surgery under general anesthesia. In addition, cost savings using the cervical block are evaluated (due to reduced length of hospital stay).

The study is prospective, randomized, double blind, and placebo-controlled. The study is performed at the Department of Surgery, Cantonal Hospital of St. Gallen.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Thyroidectomy

Clinical Trial Details

NCT number	NCT00472446
Study type	Interventional
Source	Cantonal Hospital of St. Gallen
Contact
Status	Completed
Phase	Phase 2/Phase 3
Start date	January 2006
Completion date	December 2008

View Details

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