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Auricular Acupuncture for The Treatment of Post-Tonsillectomy Pain

Auricular Acupuncture for The Treatment of Post-Tonsillectomy Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01790477
Enrollment
134
Registered
2013-02-13
Start date
2012-11-30
Completion date
2015-02-28
Last updated
2016-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea, Peritonsillar Abscess, Recurrent Tonsillitis

Keywords

Tonsillectomy, Acupuncture

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.

Interventions

PROCEDUREAuricular Acupuncture

Application of auricular acupuncture to 5 points on the ear

Sponsors

United States Naval Medical Center, San Diego
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
Reduction in VAS scores between experimental and control group2 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026