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Efficacy of selenium supplementation for mild-to-moderate Graves’ ophthalmopathy in a selenium-sufficient area (SeGOSS trial): study protocol for a phase III, multicenter, open-label, randomized, controlled intervention trial
by
Jung, Kyong Yeun
, Park, Young Joo
, Ahn, Hwa Young
, Chung, Chae Won
, Jung, Eun Hye
, Lee, Min Joung
, Lee, Jeong Kyu
, Cho, Sun Wook
in
Biomedicine
/ Clinical trials
/ Clinical Trials, Phase III as Topic
/ Diagnosis
/ Dietary supplements
/ Dietary Supplements - adverse effects
/ Drug therapy
/ Eyes & eyesight
/ Graves Ophthalmopathy - diagnosis
/ Graves Ophthalmopathy - drug therapy
/ Graves’ disease
/ Graves’ ophthalmopathy (GO)
/ Health Sciences
/ Humans
/ Inflammatory diseases
/ Medicine
/ Medicine & Public Health
/ Multicenter Studies as Topic
/ Prospective Studies
/ Quality of Life
/ Randomized Controlled Trials as Topic
/ Selenium
/ Selenium - adverse effects
/ Statistics for Life Sciences
/ Study Protocol
/ Thyroid eye disease
/ Vitamin B Complex - therapeutic use
2023
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Efficacy of selenium supplementation for mild-to-moderate Graves’ ophthalmopathy in a selenium-sufficient area (SeGOSS trial): study protocol for a phase III, multicenter, open-label, randomized, controlled intervention trial
by
Jung, Kyong Yeun
, Park, Young Joo
, Ahn, Hwa Young
, Chung, Chae Won
, Jung, Eun Hye
, Lee, Min Joung
, Lee, Jeong Kyu
, Cho, Sun Wook
in
Biomedicine
/ Clinical trials
/ Clinical Trials, Phase III as Topic
/ Diagnosis
/ Dietary supplements
/ Dietary Supplements - adverse effects
/ Drug therapy
/ Eyes & eyesight
/ Graves Ophthalmopathy - diagnosis
/ Graves Ophthalmopathy - drug therapy
/ Graves’ disease
/ Graves’ ophthalmopathy (GO)
/ Health Sciences
/ Humans
/ Inflammatory diseases
/ Medicine
/ Medicine & Public Health
/ Multicenter Studies as Topic
/ Prospective Studies
/ Quality of Life
/ Randomized Controlled Trials as Topic
/ Selenium
/ Selenium - adverse effects
/ Statistics for Life Sciences
/ Study Protocol
/ Thyroid eye disease
/ Vitamin B Complex - therapeutic use
2023
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Efficacy of selenium supplementation for mild-to-moderate Graves’ ophthalmopathy in a selenium-sufficient area (SeGOSS trial): study protocol for a phase III, multicenter, open-label, randomized, controlled intervention trial
by
Jung, Kyong Yeun
, Park, Young Joo
, Ahn, Hwa Young
, Chung, Chae Won
, Jung, Eun Hye
, Lee, Min Joung
, Lee, Jeong Kyu
, Cho, Sun Wook
in
Biomedicine
/ Clinical trials
/ Clinical Trials, Phase III as Topic
/ Diagnosis
/ Dietary supplements
/ Dietary Supplements - adverse effects
/ Drug therapy
/ Eyes & eyesight
/ Graves Ophthalmopathy - diagnosis
/ Graves Ophthalmopathy - drug therapy
/ Graves’ disease
/ Graves’ ophthalmopathy (GO)
/ Health Sciences
/ Humans
/ Inflammatory diseases
/ Medicine
/ Medicine & Public Health
/ Multicenter Studies as Topic
/ Prospective Studies
/ Quality of Life
/ Randomized Controlled Trials as Topic
/ Selenium
/ Selenium - adverse effects
/ Statistics for Life Sciences
/ Study Protocol
/ Thyroid eye disease
/ Vitamin B Complex - therapeutic use
2023
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Efficacy of selenium supplementation for mild-to-moderate Graves’ ophthalmopathy in a selenium-sufficient area (SeGOSS trial): study protocol for a phase III, multicenter, open-label, randomized, controlled intervention trial
Journal Article
Efficacy of selenium supplementation for mild-to-moderate Graves’ ophthalmopathy in a selenium-sufficient area (SeGOSS trial): study protocol for a phase III, multicenter, open-label, randomized, controlled intervention trial
2023
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Overview
Background
The therapeutic effect of selenium has been demonstrated in mild Graves’ ophthalmopathy (GO) in a European region where selenium status is suboptimal. However, there is a lack of evidence to support selenium use in selenium-sufficient areas. The aim of this study is to evaluate the therapeutic effect of selenium in mild-to-moderate GO in selenium-sufficient South Korea.
Methods
The SeGOSS trial is a multicenter, prospective, randomized, open-label trial in South Korea. Eighty-four patients aged 19 years or older with mild-to-moderate GO will be randomized to receive either vitamin B complex alone or vitamin B complex with selenium for 6 months with three monthly follow-up visits. The primary outcome is comparison of the improvement in quality of life at 6 months from baseline between the control and selenium groups. The secondary outcomes are intergroup differences in changes in quality of life at 3 months, clinical activity of GO at 3 and 6 months, thyroid autoantibody titers at 3 and 6 months, and the response rate at 3 and 6 months from baseline. Quality of life will be measured by questionnaire for patients with GO, and the clinical activity of GO will be evaluated by the clinical activity score (CAS). A positive response is defined as either changes in the CAS < 0 or the changes in the GO-QOL score ≥ 6.
Discussion
The SeGOSS study will evaluate the therapeutic potential of selenium for mild-to-moderate GO in a selenium-sufficient area and provide support in tailoring better treatment for GO.
Trial registration
KCT0004040. Retrospectively registered on 5 June 2019.
https://cris.nih.go.kr/cris/search/detailSearch.do/14160
.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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