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Acupuncture Treatment of Dry Eye

Not Applicable
Completed
Conditions
Keratoconjunctivitis Sicca
Xeropthalmia
Interventions
Procedure: Acupuncture
Procedure: Sham acupuncture
Registration Number
NCT00554879
Lead Sponsor
Walter Reed Army Medical Center
Brief Summary

The purpose of this study is to determine the safety and efficacy of acupuncture in the treatment of moderate to severe dry eye by replicating the study design of the previous protocol and to see the study through to its completion.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Military healthcare beneficiary
  • Male and female patients, at least 18 years of age
  • Diagnosis of keratoconjunctivitis sicca or xerophthalmia (dry eyes) in one or both eyes
  • Persistent signs and symptoms despite conventional therapy for at least three months
Exclusion Criteria
  • Contact lens wear
  • Intraocular surgery or laser in the study eye within 90 days prior to enrolling in the study
  • History of any medical condition or circumstance that would preclude scheduled visits or completion of the study
  • Known history of adverse reaction to acupuncture
  • Pregnancy or breast feeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1AcupunctureAcupuncture
2Sham acupunctureSham Acupuncture
Primary Outcome Measures
NameTimeMethod
To answer the question of whether there are objective beneficial effects of an acupuncture treatment versus sham acupuncture on dry eye, as measured by some of the most widely-used clinical indicators in the literature.6 months after acupuncture or sham acupuncture treatment
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Walter Reed Army Medical Center

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Washington DC, District of Columbia, United States

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