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Analgesic Effect of Intraoperative Esmolol in Mastectomies

NCT02466542 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2017-04-05

No results posted yet for this study

Summary

This study aims to compare the quality of perioperative analgesia of esmolol in patients undergoing mastectomy.

Conditions

  • Postoperative Pain

Interventions

DRUG

Placebo group

Patients will receive regular general anesthesia

DRUG

Esmolol group

Patients will receive regular general anesthesia plus esmolol infusion

Sponsors & Collaborators

  • Hospital de Base

    lead OTHER

Principal Investigators

  • Fabricio T Mendonca, MD, TSA · Hospital de Base do Distrito Federal

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2017-02-28
Completion
2017-02-28

Countries

  • Brazil

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 NCT02466542 on ClinicalTrials.gov