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Evaluation of a new artificial tear formulation for the management of tear film stability and visual function in patients with dry eye
Artificial tears are the first line of therapy for dry eye disease (DED) and are also the most frequently used treatment approach for this common condition. Despite this, there are few published studies that directly compare the effectiveness of different drop preparations, especially those formulat...
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Published in: | Clinical ophthalmology (Auckland, N.Z.) N.Z.), 2017-01, Vol.11, p.1883-1889 |
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creator | Torkildsen, Gail Brujic, Mile Cooper, Michael S Karpecki, Paul Majmudar, Parag Trattler, William Reis, Meryl Ciolino, Joseph B |
description | Artificial tears are the first line of therapy for dry eye disease (DED) and are also the most frequently used treatment approach for this common condition. Despite this, there are few published studies that directly compare the effectiveness of different drop preparations, especially those formulated specifically for dry eye. In this study, we tested a new artificial tear product, Rohto
Dry-Aid™, for its ability to relieve the signs and symptoms of DED. The study used a second drop, Systane
Ultra, as a positive comparator.
This was a prospective, single-center, open-label, parallel-group study comparing the effects of the two products when used continuously over ~30 days (Clinical Trials registration number NCT03183089). Subjects were randomly assigned to one of the two test groups and were monitored 2 and 4 weeks after enrollment. Efficacy endpoints included ocular staining, visual function, and ocular discomfort.
Treatment groups had similar ocular staining and ocular comfort scores, and both showed statistically significant ocular discomfort score improvement. Subjects in the Rohto group reported significant improvements in visual tasking activities such as watching television and driving at night. There was also a tendency for diary symptom scores to worsen from morning to evening in the Systane group, but not in the Rohto group; this trend was not significant, but warrants further study.
The two products, Rohto Dry-Aid and Systane Ultra, elicited comparable effects on the signs and symptoms of DED. While both products are designed to provide long-lasting relief, subjects in the Rohto group experienced a superior relief from discomfort associated with visual tasking activities and daily diaries, indicating that the Rohto drops may provide a longer duration of symptomatic relief over the course of the day. |
doi_str_mv | 10.2147/OPTH.S144369 |
format | article |
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Dry-Aid™, for its ability to relieve the signs and symptoms of DED. The study used a second drop, Systane
Ultra, as a positive comparator.
This was a prospective, single-center, open-label, parallel-group study comparing the effects of the two products when used continuously over ~30 days (Clinical Trials registration number NCT03183089). Subjects were randomly assigned to one of the two test groups and were monitored 2 and 4 weeks after enrollment. Efficacy endpoints included ocular staining, visual function, and ocular discomfort.
Treatment groups had similar ocular staining and ocular comfort scores, and both showed statistically significant ocular discomfort score improvement. Subjects in the Rohto group reported significant improvements in visual tasking activities such as watching television and driving at night. There was also a tendency for diary symptom scores to worsen from morning to evening in the Systane group, but not in the Rohto group; this trend was not significant, but warrants further study.
The two products, Rohto Dry-Aid and Systane Ultra, elicited comparable effects on the signs and symptoms of DED. While both products are designed to provide long-lasting relief, subjects in the Rohto group experienced a superior relief from discomfort associated with visual tasking activities and daily diaries, indicating that the Rohto drops may provide a longer duration of symptomatic relief over the course of the day.</description><identifier>ISSN: 1177-5467</identifier><identifier>ISSN: 1177-5483</identifier><identifier>EISSN: 1177-5483</identifier><identifier>DOI: 10.2147/OPTH.S144369</identifier><identifier>PMID: 29089744</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Aging ; artificial tears ; blurred vision ; Care and treatment ; Clinical Trial Report ; Cornea ; Diabetes ; Diagnosis ; dry eye ; Epidemiology ; Eye diseases ; Health aspects ; Laboratories ; Lipids ; Lubricants & lubrication ; Ophthalmology ; Signs and symptoms ; tear film ; Vision ; visual function</subject><ispartof>Clinical ophthalmology (Auckland, N.Z.), 2017-01, Vol.11, p.1883-1889</ispartof><rights>COPYRIGHT 2017 Dove Medical Press Limited</rights><rights>2017. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Torkildsen et al. This work is published and licensed by Dove Medical Press Limited 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c576t-e0db004e4bd9556001f12b80390ba945f28b035252cd9b8fdcb7afc5c97bcaad3</citedby><orcidid>0000-0003-2344-5048</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2225030573/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2225030573?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29089744$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Torkildsen, Gail</creatorcontrib><creatorcontrib>Brujic, Mile</creatorcontrib><creatorcontrib>Cooper, Michael S</creatorcontrib><creatorcontrib>Karpecki, Paul</creatorcontrib><creatorcontrib>Majmudar, Parag</creatorcontrib><creatorcontrib>Trattler, William</creatorcontrib><creatorcontrib>Reis, Meryl</creatorcontrib><creatorcontrib>Ciolino, Joseph B</creatorcontrib><title>Evaluation of a new artificial tear formulation for the management of tear film stability and visual function in patients with dry eye</title><title>Clinical ophthalmology (Auckland, N.Z.)</title><addtitle>Clin Ophthalmol</addtitle><description>Artificial tears are the first line of therapy for dry eye disease (DED) and are also the most frequently used treatment approach for this common condition. Despite this, there are few published studies that directly compare the effectiveness of different drop preparations, especially those formulated specifically for dry eye. In this study, we tested a new artificial tear product, Rohto
Dry-Aid™, for its ability to relieve the signs and symptoms of DED. The study used a second drop, Systane
Ultra, as a positive comparator.
This was a prospective, single-center, open-label, parallel-group study comparing the effects of the two products when used continuously over ~30 days (Clinical Trials registration number NCT03183089). Subjects were randomly assigned to one of the two test groups and were monitored 2 and 4 weeks after enrollment. Efficacy endpoints included ocular staining, visual function, and ocular discomfort.
Treatment groups had similar ocular staining and ocular comfort scores, and both showed statistically significant ocular discomfort score improvement. Subjects in the Rohto group reported significant improvements in visual tasking activities such as watching television and driving at night. There was also a tendency for diary symptom scores to worsen from morning to evening in the Systane group, but not in the Rohto group; this trend was not significant, but warrants further study.
The two products, Rohto Dry-Aid and Systane Ultra, elicited comparable effects on the signs and symptoms of DED. While both products are designed to provide long-lasting relief, subjects in the Rohto group experienced a superior relief from discomfort associated with visual tasking activities and daily diaries, indicating that the Rohto drops may provide a longer duration of symptomatic relief over the course of the day.</description><subject>Aging</subject><subject>artificial tears</subject><subject>blurred vision</subject><subject>Care and treatment</subject><subject>Clinical Trial Report</subject><subject>Cornea</subject><subject>Diabetes</subject><subject>Diagnosis</subject><subject>dry eye</subject><subject>Epidemiology</subject><subject>Eye diseases</subject><subject>Health aspects</subject><subject>Laboratories</subject><subject>Lipids</subject><subject>Lubricants & lubrication</subject><subject>Ophthalmology</subject><subject>Signs and symptoms</subject><subject>tear film</subject><subject>Vision</subject><subject>visual function</subject><issn>1177-5467</issn><issn>1177-5483</issn><issn>1177-5483</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1rFDEUhgdRbK3eeS0BQbxw13xOZm4KpVRbKFSwXodMPnazZJI1mdmyf8Dfbaa7rl2RXCTMPO8TzsmpqrcIzjGi_PPdt_vr-XdEKanbZ9UpQpzPGG3I88O55ifVq5xXENYYNvxldYJb2LSc0tPq19VG-lEOLgYQLZAgmAcg0-CsU056MBiZgI2pH_0OKmcwLA3oZZAL05swTLkd5nwP8iA7592wBTJosHF5LBY7BvWYdgGsi6ekMnhwwxLotAVma15XL6z02bzZ72fVjy9X95fXs9u7rzeXF7czxXg9zAzUHYTU0E63jNUQIotw10DSwk62lFncdJAwzLDSbddYrTourWKq5Z2SUpOz6mbn1VGuxDq5XqatiNKJxw8xLcRUvPJGcINZ09i6JaSmBNYSYo2YQYp0uvRUFtf5zrUeu95oVYpK0h9Jj_8EtxSLuBGsZjWhrAg-7gUp_hxNHkTvsjLey2DimAVqWcMo47Ap6Pt_0FUcUyitEhhjBglknPylFrIU4IKN5V41ScUFIwgjjlpcqPl_qLK06Z2KwZR3NMeBD08CSyP9sMzRj9OL5mPw0w5UKeacjD00A0ExDauYhlXsh7Xg75428AD_mU7yG2CF5MQ</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Torkildsen, Gail</creator><creator>Brujic, Mile</creator><creator>Cooper, Michael S</creator><creator>Karpecki, Paul</creator><creator>Majmudar, Parag</creator><creator>Trattler, William</creator><creator>Reis, Meryl</creator><creator>Ciolino, Joseph B</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-2344-5048</orcidid></search><sort><creationdate>20170101</creationdate><title>Evaluation of a new artificial tear formulation for the management of tear film stability and visual function in patients with dry eye</title><author>Torkildsen, Gail ; 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Despite this, there are few published studies that directly compare the effectiveness of different drop preparations, especially those formulated specifically for dry eye. In this study, we tested a new artificial tear product, Rohto
Dry-Aid™, for its ability to relieve the signs and symptoms of DED. The study used a second drop, Systane
Ultra, as a positive comparator.
This was a prospective, single-center, open-label, parallel-group study comparing the effects of the two products when used continuously over ~30 days (Clinical Trials registration number NCT03183089). Subjects were randomly assigned to one of the two test groups and were monitored 2 and 4 weeks after enrollment. Efficacy endpoints included ocular staining, visual function, and ocular discomfort.
Treatment groups had similar ocular staining and ocular comfort scores, and both showed statistically significant ocular discomfort score improvement. Subjects in the Rohto group reported significant improvements in visual tasking activities such as watching television and driving at night. There was also a tendency for diary symptom scores to worsen from morning to evening in the Systane group, but not in the Rohto group; this trend was not significant, but warrants further study.
The two products, Rohto Dry-Aid and Systane Ultra, elicited comparable effects on the signs and symptoms of DED. While both products are designed to provide long-lasting relief, subjects in the Rohto group experienced a superior relief from discomfort associated with visual tasking activities and daily diaries, indicating that the Rohto drops may provide a longer duration of symptomatic relief over the course of the day.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>29089744</pmid><doi>10.2147/OPTH.S144369</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-2344-5048</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aging artificial tears blurred vision Care and treatment Clinical Trial Report Cornea Diabetes Diagnosis dry eye Epidemiology Eye diseases Health aspects Laboratories Lipids Lubricants & lubrication Ophthalmology Signs and symptoms tear film Vision visual function |
title | Evaluation of a new artificial tear formulation for the management of tear film stability and visual function in patients with dry eye |
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