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UnknownNCT01171885

Bilateral Superficial Cervical Block for Thyroidectomy

Evaluation of the Postoperative Analgesic Efficacy of Bilateral Superficial Cervical Block for Thyroidectomy and Mini Incision Under General Balanced Anesthesia: a Randomized, Triple Masked, Placebo Controlled Trial.

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Lifecenter Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to compare the postoperative analgesia afforded by bilateral superficial cervical block using different concentrations of local anesthetic (ropivacaine) in patients undergoing total thyroidectomy for the mini-incision technique, performed by the same surgical team.

Detailed description

In this study we will evaluate the efficacy of bilateral superficial cervical block associated with balanced general anesthesia with remifentanil as opioid of choice in preventing postoperative pain in patients who underwent total thyroidectomy with mini incision without neck dissection.A hundred and twenty patients ASA I - II will be assessed and allocated randomly (through a table of random numbers) into three groups for analgesia for post-operative: Group 1: bilateral superficial cervical block with 20 ml of 0.9% saline (placebo); Group 2: bilateral superficial cervical block with 20 ml ropivacaine 0.25%; Group 3: bilateral superficial cervical block with 20 ml ropivacaine 0.5%.

Conditions

Interventions

TypeNameDescription
DRUG0.9% saline20 ml of 0.9% saline
DRUGRopivacaine20 ml of Ropivacaine 0.25%.
DRUGRopivacaine20 ml of Ropivacaine 0.5%.

Timeline

Start date
2009-07-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2010-07-29
Last updated
2010-07-29

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01171885. Inclusion in this directory is not an endorsement.