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Acupuncture for Dry Eye

Phase 3
Completed
Conditions
Dry Eye
Interventions
Device: Acupuncture
Drug: Refresh Plus
Registration Number
NCT01105221
Lead Sponsor
Korea Institute of Oriental Medicine
Brief Summary

The purpose of this study is to assess whether acupuncture is more effective than artificial tear drop in the treatment of dry eye.

Detailed Description

Dry eye is one of the common diseases in ophthalmology. It affects not only patients' daily activities such as reading, carrying out professional work, using the computer, watching television, and driving, but also bodily health conditions such as bodily pain, discomfort and lower energy and vitality.

Currently, artificial tears are easily subscribed or used in the shape of OTC drugs. However, preservatives in artificial tears may exacerbate ocular surface inflammation and the safety of anti-inflammatory treatment is not well established.

Acupuncture, one of the most popular CAM interventions, showed some favourable effects over artificial tears for dry eye in several randomised controlled trials (RCTs). The evidence obtained from these trials is quite limited because all of these RCTs were conducted under high risk of biases. Therefore, well-designed RCTs are needed to establish the efficacy of acupuncture for dry eye.

In a clinical trial, cost-effectiveness and qualitative researches can be carried out parallely. Through this kind of mixed method approaches, various compartments, consisting acupuncture treatment effects are able to be revealed totally.

In this context, the investigators designed a multi-center randomized controlled trial, comparing acupuncture treatment and artificial tear drop with immunoassay for the change of tear cytokine concentration, cost effectiveness study and qualitative research in a mixed method approach.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Patients who have had dry eye syndromes in single eye or in both eyes (ICD-10 : H04.1). He or she must have both of the conditions below:

    1. Patients who have dry eye symptoms such as itching, ocular foreign body sensation, ocular burning, ocular pain, ocular dryness, blurred vision, sensation of photophobia, ocular redness, sensation of tearing
    2. Patients whose tear film break-up time is below 10 seconds and Schirmer I test results is below 10mm/5sec.
Exclusion Criteria
  • Patients who have defects of the eyelid or eyelashes
  • Acute infection of the eyelid, eyeball or eye accessories
  • Stevens-Johnson syndrome
  • Vitamin A deficiency
  • Eye or accessory defects due to external injuries
  • A past history of surgical operation related to the eye in last three months
  • Punctual occlusion
  • Current usage of contact lenses
  • Sequelae of facial palsy,
  • Current usage of anti-inflammatory eye drops in the last two weeks
  • Pregnancy
  • Using history of traditional medicinal treatment such as acupuncture, moxibustion and herbal medicine in the last one month

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
AcupunctureAcupuncture-
Artificial tear dropRefresh Plus-
Primary Outcome Measures
NameTimeMethod
Ocular Surface Disease Index (OSDI)Up to 13 weeks

This questionnaire is a 12-item instrument for ocular irritation and impact on visual function in dry eye sufferers. It can provide quantifiable results of dry eye symptom frequency and vision-related functioning. Korean version of the OSDI questionnaire will be used. Follow up measurement will be assessed after 4, 5, 9 and 13 weeks from the first visit.

Secondary Outcome Measures
NameTimeMethod
Visual analogue scale (VAS) for self-assessment of ocular discomfortUp to 13 weeks

Self-reports on ocular symptoms concomitant with dry eye, such conditions as ocular itching, foreign body sensation, burning, pain and dryness as well as for blurred vision, sensation of photophobia, ocular redness and sensation of tearing. Follow up measurement will be assessed after 4, 5, 9 and 13 weeks from the first visit.

Schirmer I test with anaesthesiaUp to 13 weeks

This ia a method for checking basic tear secretion. Schirmer test paper (Color Bar™ Eagle Vision, USA) will be inserted on the lateral third of the lower eyelid with the participant's eye closed for five minutes. Follow up measurement will be assessed after 5 weeks and 13 weeks from the first visit.

Tear Film Break Up Time (BUT)Up to 13 weeks

This is a method for observing tear film stability. Sodium fluorescein (2.5%) will be instilled in both eyes and the tear break-up time (the interval between the last complete blink and the first appearance of a dry spot or disruption in the tear film) will be measured. Follow up measurement will be assessed after 5 weeks and 13 weeks from the first visit.

General Assessment by acupuncture practitioner and participantsUp to 5 weeks

Practitioners and participants will evaluate the improvement of ocular symptoms after treatment. They can chose one of the following 5 grades: Excellent, Good, Fair, Poor and Aggravation.

Self reports about experiences of using other dry eye-related treatments after the end of each intervention.Up to 13 weeks

For cost-effective analysis, all experience of using other dry eye-related treatments after the end of each intervention should be reported by participants. It contains frequency of hospital visit and treatments methods. Follow up measurement will be assessed after 9, 13 weeks from the first visit.

Quality of life (QOL)Up to 13 weeks

One questionaire for QOL, related to dry eye, is asked. Follow up measurement will be assessed after 4, 5, 9 and 13 weeks from the first visit.

Case reports on adverse events for the evaluation of safetyUp to 13 weeks

Adverse events, adverse acupuncture or artificial tear drop reaction, serious and unexpected adverse acupuncture or artificial tear drop reaction and serious adverse event will be reported by participants and checked by practioners in every visit. Number of participants with adverse events will also be recorded.

Qualitative analysis (additional study)Up to 13 weeks

Questionaires with open-ended question about personal experiences for dry eye, acupuncture treatment and usage of artificial tear drop will be distributed to every participant of both group. Follow up measurement will be assessed after 4 and 13 weeks from the first visit.

Cost-effectiveness analysis between acupuncture and artificial tear drop treatment (additional study)Up to 13 weeks

Cost-effectiveness of acupucnture will be analyzed using Ocular Surface Disease Index (OSDI) variable, comparing the cost of artificial tear drops. the Cost which all participants will use for dry eye during the trial period, will be recorded in every visit.

Trial Locations

Locations (3)

Clinical Research Center of DongGuk Univ. Internaltional Hospital

🇰🇷

Goyang, Gyeonggi, Korea, Republic of

Clinical Research Center of Korea Institute of Oriental Medicine

🇰🇷

Daejeon, Korea, Republic of

Clinical Research Center of DongShin Univ. Oriental Hospital

🇰🇷

Gwangju, Korea, Republic of

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