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Clinical Trials/NCT01790477
NCT01790477
Completed
Not Applicable

Auricular Acupuncture for The Treatment of Post-Tonsillectomy Pain

United States Naval Medical Center, San Diego1 site in 1 country134 target enrollmentNovember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Recurrent Tonsillitis
Sponsor
United States Naval Medical Center, San Diego
Enrollment
134
Locations
1
Primary Endpoint
Reduction in VAS scores between experimental and control group
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The goal of this study is to assess the role of battlefield acupuncture in the reduction of pain scores status post adult tonsillectomy. Secondary goals of this study include reduction in narcotic usage, decreased nausea and vomiting, and evaluating patient factors that lend an increased risk of worsening pain or improved response with acupuncture.

Registry
clinicaltrials.gov
Start Date
November 2012
End Date
February 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
United States Naval Medical Center, San Diego
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Any adult patient who meets criteria and is scheduled for tonsillectomy

Exclusion Criteria

  • Any patient with prior use of acupuncture
  • Individuals under age 18
  • Tonsillectomy performed with other surgical procedures, i.e UPPP, adenoidectomy,
  • Patients with a known personal or family history of a bleeding disorder will be excluded.
  • Patients with a history of kidney or liver problems will also be excluded.
  • Patients found to be pregnant will be excluded from participation.
  • Patients unwilling to enroll in the study will have the tonsillectomy with or without adenoidectomy performed according to current practice standards.

Outcomes

Primary Outcomes

Reduction in VAS scores between experimental and control group

Time Frame: 2 weeks

Study Sites (1)

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