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Acupuncture for dry eye: a randomised controlled trial protocol

BACKGROUND: Dry eye is usually managed by conventional medical interventions such as artificial tears, anti-inflammatory drugs and surgical treatment. However, since dry eye is one of the most frequent ophthalmologic disorders, safer and more effective methods for its treatment are necessary, especi...

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Autores principales: Kim, Tae-Hun, Kim, Jong-In, Shin, Mi-Suk, Lee, Myeong Soo, Choi, Jun-Yong, Jung, So-Yong, Kim, Ae-Ran, Seol, Jae-Uk, Choi, Sun-Mi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797009/
https://www.ncbi.nlm.nih.gov/pubmed/19958541
http://dx.doi.org/10.1186/1745-6215-10-112
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author Kim, Tae-Hun
Kim, Jong-In
Shin, Mi-Suk
Lee, Myeong Soo
Choi, Jun-Yong
Jung, So-Yong
Kim, Ae-Ran
Seol, Jae-Uk
Choi, Sun-Mi
author_facet Kim, Tae-Hun
Kim, Jong-In
Shin, Mi-Suk
Lee, Myeong Soo
Choi, Jun-Yong
Jung, So-Yong
Kim, Ae-Ran
Seol, Jae-Uk
Choi, Sun-Mi
author_sort Kim, Tae-Hun
collection PubMed
description BACKGROUND: Dry eye is usually managed by conventional medical interventions such as artificial tears, anti-inflammatory drugs and surgical treatment. However, since dry eye is one of the most frequent ophthalmologic disorders, safer and more effective methods for its treatment are necessary, especially for vulnerable patients. Acupuncture has been widely used to treat patients with dry eye. Our aim is to evaluate the effectiveness and safety of acupuncture for this condition. METHODS/DESIGN: A randomised, patient-assessor blinded, sham (non-acupuncture point, shallow acupuncture) controlled study was established. Participants allocated to verum acupuncture and sham acupuncture groups will be treated three times weekly for three weeks for a total of nine sessions per participant. Seventeen points (GV23; bilateral BL2, GB4, TE23, Ex1 (Taiyang), ST1 and GB20; and left SP3, LU9, LU10 and HT8 for men, right for women) have been selected for the verum acupuncture; for the sham acupuncture, points have been selected that do not coincide with a classical acupuncture point and that are located close to the verum points, except in the case of the rim of the eye. Ocular surface disease index, tear film breakup time, the Schirmer I test, medication quantification scale and general assessment of improvement will be used as outcome variables for evaluating the effectiveness of acupuncture. Safety will also be assessed at every visit. Primary and secondary outcomes will be assessed four weeks after screening. All statistical analyses will be performed using analysis of covariance. DISCUSSION: The results of this trial will be used as a basis for clarifying the efficacy of acupuncture for dry eye. TRIAL REGISTRATION: ClinicalTrials.gov NCT00969280.
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spelling pubmed-27970092009-12-23 Acupuncture for dry eye: a randomised controlled trial protocol Kim, Tae-Hun Kim, Jong-In Shin, Mi-Suk Lee, Myeong Soo Choi, Jun-Yong Jung, So-Yong Kim, Ae-Ran Seol, Jae-Uk Choi, Sun-Mi Trials Study protocol BACKGROUND: Dry eye is usually managed by conventional medical interventions such as artificial tears, anti-inflammatory drugs and surgical treatment. However, since dry eye is one of the most frequent ophthalmologic disorders, safer and more effective methods for its treatment are necessary, especially for vulnerable patients. Acupuncture has been widely used to treat patients with dry eye. Our aim is to evaluate the effectiveness and safety of acupuncture for this condition. METHODS/DESIGN: A randomised, patient-assessor blinded, sham (non-acupuncture point, shallow acupuncture) controlled study was established. Participants allocated to verum acupuncture and sham acupuncture groups will be treated three times weekly for three weeks for a total of nine sessions per participant. Seventeen points (GV23; bilateral BL2, GB4, TE23, Ex1 (Taiyang), ST1 and GB20; and left SP3, LU9, LU10 and HT8 for men, right for women) have been selected for the verum acupuncture; for the sham acupuncture, points have been selected that do not coincide with a classical acupuncture point and that are located close to the verum points, except in the case of the rim of the eye. Ocular surface disease index, tear film breakup time, the Schirmer I test, medication quantification scale and general assessment of improvement will be used as outcome variables for evaluating the effectiveness of acupuncture. Safety will also be assessed at every visit. Primary and secondary outcomes will be assessed four weeks after screening. All statistical analyses will be performed using analysis of covariance. DISCUSSION: The results of this trial will be used as a basis for clarifying the efficacy of acupuncture for dry eye. TRIAL REGISTRATION: ClinicalTrials.gov NCT00969280. BioMed Central 2009-12-03 /pmc/articles/PMC2797009/ /pubmed/19958541 http://dx.doi.org/10.1186/1745-6215-10-112 Text en Copyright ©2009 Kim et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study protocol
Kim, Tae-Hun
Kim, Jong-In
Shin, Mi-Suk
Lee, Myeong Soo
Choi, Jun-Yong
Jung, So-Yong
Kim, Ae-Ran
Seol, Jae-Uk
Choi, Sun-Mi
Acupuncture for dry eye: a randomised controlled trial protocol
title Acupuncture for dry eye: a randomised controlled trial protocol
title_full Acupuncture for dry eye: a randomised controlled trial protocol
title_fullStr Acupuncture for dry eye: a randomised controlled trial protocol
title_full_unstemmed Acupuncture for dry eye: a randomised controlled trial protocol
title_short Acupuncture for dry eye: a randomised controlled trial protocol
title_sort acupuncture for dry eye: a randomised controlled trial protocol
topic Study protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797009/
https://www.ncbi.nlm.nih.gov/pubmed/19958541
http://dx.doi.org/10.1186/1745-6215-10-112
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