The Effect of Electroacustimulation on Postoperative Nausea, Vomiting and Pain in Outpatient Plastic Surgery Patients

University of Wisconsin (UW)

Status: Completed

Conditions: Postoperative Nausea and Vomiting

Treatments: Device: Electroacustimulation

Study type: Interventional

Funder types: Other

Identifiers

NCT00941005

H-2007-0100

Details and patient eligibility

About

Introduction: Current rates of postoperative nausea and vomiting (PONV) experienced by outpatient surgery patients are as high as 20-30%. Electroacustimulation (EAS) therapy has been demonstrated to be effective in controlling these symptoms, but trials identifying their efficacy in the outpatient surgery population are lacking. This study integrates conventional pharmacotherapy with alternative medicine in prevention of PONV.

Materials and Methods: One hundred twenty two patients undergoing surgery procedures at an outpatient surgery center were randomized to two treatment arms. The first arm was standardized pharmacologic PONV prevention typical for patients undergoing outpatient surgery, while the second arm employed the use of ReliefBand, an FDA-approved electroacustimulation (EAS) device with pharmacologic treatment to relieve symptoms of PONV and pain. EAS is a derivative of acupuncture therapy that uses a small electrical current to stimulate acupuncture points on the human body and is thought to relieve nausea, vomiting and pain. Outcomes measured were post-op questionnaires evaluating pain and nausea symptoms, emetic events, the need for rescue medications and the time to discharge.

Enrollment: 122 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• undergoing surgery at the University of Wisconsin outpatient surgery center

Exclusion criteria

• pregnancy
• currently experiencing menstrual symptoms
• cardiac pacemaker
• previous experience with acupuncture therapy
• pharmacologic treatment for nausea or vomiting in the 24 hours prior to surgery

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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122 participants in 2 patient groups

Electroacustimulation

Experimental group

Description:

Received electroacustimulation at the wrist using a small, battery-powered electroacustimulation device.

Treatment:

Device: Electroacustimulation

Control

Sham Comparator group

Description:

Received a device that was not turned on.

Treatment:

Device: Electroacustimulation