Acupuncture for Dry Eye

Dry Eye Clinical Trial

Official title:

Acupuncture for Dry Eye: a Multicenter Randomized Controlled Trial With Active Comparison Intervention (Artificial Tear Drop) Using a Mixed Method Approach

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01105221
• Other study ID #: KI1001
• Status: Completed
• Phase: Phase 3
• First received: April 13, 2010
• Last updated: January 7, 2011
• Start date: April 2010
• Est. completion date: January 2011

Study information

• Verified date: April 2010
• Source: Korea Institute of Oriental Medicine
• Contact: n/a
• Is FDA regulated: No
• Health authority: South Korea: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

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

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 information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: January 2011
• Est. primary completion date: November 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 19 Years to 65 Years

Eligibility

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

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Dry Eye
• Dry Eye Syndromes
• Keratoconjunctivitis Sicca

Intervention

Device:
• Acupuncture
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.

Drug:
• Refresh Plus
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.

Locations

Country	Name	City	State
Korea, Republic of	Clinical Research Center of Korea Institute of Oriental Medicine	Daejeon
Korea, Republic of	Clinical Research Center of DongGuk Univ. Internaltional Hospital	Goyang	Gyeonggi
Korea, Republic of	Clinical Research Center of DongShin Univ. Oriental Hospital	Gwangju

Sponsors (3)

Lead Sponsor	Collaborator
Korea Institute of Oriental Medicine	DongGuk University, DONGSHIN University Oriental Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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.	Up to 13 weeks	No
Secondary	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.	Up to 13 weeks	No
Secondary	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.	Up to 13 weeks	No
Secondary	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.	Up to 13 weeks	No
Secondary	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.	Up to 5 weeks	No
Secondary	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.	Up to 13 weeks	No
Secondary	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.	Up to 13 weeks	No
Secondary	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.	Up to 13 weeks	Yes
Secondary	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.	Up to 13 weeks	No
Secondary	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.	Up to 13 weeks	No