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Acupuncture for Dry Eye

Primary Purpose

Dry Eye

Status
Completed
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Acupuncture
Refresh Plus
Sponsored by
Korea Institute of Oriental Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dry Eye focused on measuring Acupuncture, Dry eye, Artificial tear drop, Mixed method approach, Qualitative study, Cost effectiveness analysis, Tear cytokine analysis

Eligibility Criteria

19 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Clinical Research Center of DongGuk Univ. Internaltional Hospital
  • Clinical Research Center of Korea Institute of Oriental Medicine
  • Clinical Research Center of DongShin Univ. Oriental Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Acupuncture

Artificial tear drop

Arm Description

Outcomes

Primary Outcome Measures

Ocular Surface Disease Index (OSDI)
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

Visual analogue scale (VAS) for self-assessment of ocular discomfort
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 anaesthesia
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)
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 participants
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.
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)
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 safety
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)
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)
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.

Full Information

First Posted
April 13, 2010
Last Updated
January 7, 2011
Sponsor
Korea Institute of Oriental Medicine
Collaborators
DongGuk University, DONGSHIN University Oriental Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01105221
Brief Title
Acupuncture for Dry Eye
Official Title
Acupuncture for Dry Eye: a Multicenter Randomized Controlled Trial With Active Comparison Intervention (Artificial Tear Drop) Using a Mixed Method Approach
Study Type
Interventional

2. Study Status

Record Verification Date
April 2010
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
November 2010 (Actual)
Study Completion Date
January 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Korea Institute of Oriental Medicine
Collaborators
DongGuk University, DONGSHIN University Oriental Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye
Keywords
Acupuncture, Dry eye, Artificial tear drop, Mixed method approach, Qualitative study, Cost effectiveness analysis, Tear cytokine analysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Acupuncture
Arm Type
Experimental
Arm Title
Artificial tear drop
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
Acupuncture
Intervention Description
Participants, allocated to this group, will have twelve times of acupuncture treatment in four weeks. Seventeen acupuncture points, which are both BL2, GB14, TE23, Ex1, ST1, GB20, LI4, LI11 and single GV23, will be selected and disposable 0.20*30mm acupuncture needles(Dongbang Co., Korea) will be inserted on these points. Strong 'deqi' sensation will be induced by twisting acupuncture needles and retained for 20 minutes before removed.
Intervention Type
Drug
Intervention Name(s)
Refresh Plus
Other Intervention Name(s)
Brand name: ALLERGAN
Intervention Description
Participants, allocated to this group, will be offered preservative-free and single-use Refresh plus (Sodium carboxymethylcellulose). They should use artificial tear in both eyes at least once a day for four weeks.
Primary Outcome Measure Information:
Title
Ocular Surface Disease Index (OSDI)
Description
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.
Time Frame
Up to 13 weeks
Secondary Outcome Measure Information:
Title
Visual analogue scale (VAS) for self-assessment of ocular discomfort
Description
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.
Time Frame
Up to 13 weeks
Title
Schirmer I test with anaesthesia
Description
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.
Time Frame
Up to 13 weeks
Title
Tear Film Break Up Time (BUT)
Description
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.
Time Frame
Up to 13 weeks
Title
General Assessment by acupuncture practitioner and participants
Description
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.
Time Frame
Up to 5 weeks
Title
Self reports about experiences of using other dry eye-related treatments after the end of each intervention.
Description
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.
Time Frame
Up to 13 weeks
Title
Quality of life (QOL)
Description
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.
Time Frame
Up to 13 weeks
Title
Case reports on adverse events for the evaluation of safety
Description
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.
Time Frame
Up to 13 weeks
Title
Qualitative analysis (additional study)
Description
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.
Time Frame
Up to 13 weeks
Title
Cost-effectiveness analysis between acupuncture and artificial tear drop treatment (additional study)
Description
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.
Time Frame
Up to 13 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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: 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 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sun-Mi Choi, Dr
Organizational Affiliation
Korea Institute of Oriental Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Research Center of DongGuk Univ. Internaltional Hospital
City
Goyang
State/Province
Gyeonggi
ZIP/Postal Code
410-773
Country
Korea, Republic of
Facility Name
Clinical Research Center of Korea Institute of Oriental Medicine
City
Daejeon
ZIP/Postal Code
301-724
Country
Korea, Republic of
Facility Name
Clinical Research Center of DongShin Univ. Oriental Hospital
City
Gwangju
ZIP/Postal Code
503-232
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
22615787
Citation
Kim TH, Kang JW, Kim KH, Kang KW, Shin MS, Jung SY, Kim AR, Jung HJ, Choi JB, Hong KE, Lee SD, Choi SM. Acupuncture for the treatment of dry eye: a multicenter randomised controlled trial with active comparison intervention (artificial teardrops). PLoS One. 2012;7(5):e36638. doi: 10.1371/journal.pone.0036638. Epub 2012 May 17.
Results Reference
derived
PubMed Identifier
21078194
Citation
Kim TH, Kang JW, Kim KH, Kang KW, Shin MS, Jung SY, Kim AR, Jung HJ, Lee SD, Choi JB, Choi SM. Acupuncture for dry eye: a multicentre randomised controlled trial with active comparison intervention (artificial tear drop) using a mixed method approach protocol. Trials. 2010 Nov 16;11:107. doi: 10.1186/1745-6215-11-107.
Results Reference
derived

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Acupuncture for Dry Eye

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