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Acupuncture Treatment of Dry Eye

W

Walter Reed Army Medical Center

Status

Completed

Conditions

Xeropthalmia
Keratoconjunctivitis Sicca

Treatments

Procedure: Sham acupuncture
Procedure: Acupuncture

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT00554879
WU # 07-23024

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

20 participants in 2 patient groups

1
Experimental group
Description:
Acupuncture
Treatment:
Procedure: Acupuncture
2
Sham Comparator group
Description:
Sham Acupuncture
Treatment:
Procedure: Sham acupuncture

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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