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Clinical Trials/RBR-96h3k97
RBR-96h3k97Not yet recruitingUnknown

Effects of Transcutaneous Electrical Nerve Stimulation on the intensity of acute postoperative pain in Breast Augmentation: a randomized, placebo-controlled, double-blind clinical trial

Centro de Ciências Biológicas e da Saúde - Universidade Federal de São Carlos0 sitesStarted: February 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Unknown
Status
Not yet recruiting
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18Y to 65Y (—)
Sex
Female

Inclusion Criteria

  • Women; aged between 18 and 65; Requests for breast augmentation surgery using the 24-hour rapid recovery protocol; report a pain intensity significantly equal to or greater than 3 points on the Numerical Pain Scale in the immediate postoperative period

Exclusion Criteria

  • Chronic diseases; previous experience with electrical currents for pain; history of use of illicit and psychotropic drugs; chronic use of opioids; presence of a cardiac pacemaker; neurological disorders that interfere with the level of consciousness; changes in previous skin sensitivity in the breast; inability to support the shoulder elevated at 90 degrees

Investigators

Sponsor
Centro de Ciências Biológicas e da Saúde - Universidade Federal de São Carlos

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