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Cited 2 time in webofscience Cited 2 time in scopus
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Efficacy and safety of oxiracetam in patients with vascular cognitive impairment: A multicenter, randomized, double-blinded, placebo-controlled, phase IV clinical trial

Authors
Lim, Jae -SungLee, JuneyoungKang, YeonwookPark, Hyun-TaeKim, Dong-EogCha, Jae-KwanPark, Tai HwanHeo, Jae-HyukLee, Kyung BokPark, Jong -MooOh, Mi SunKim, Eung-GyuChang, Dae-IlHeo, Sung HyukPark, Man-SeokPark, HyunYoungYi, SangHakLee, Yeong BaePark, Kwang-YeolLee, Soo JooKim, Jae GukLee, JunCho, Kyung-HeeRha, Joung-HoKim, Yeong-InLee, Jun HongChoi, Jay CholOh, Kyung-MiKwon, Jee-HyunKim, ChulhoPark, Jong-HoJung, Keun-HwaSung, Sang MinChung, Jong-WonLee, Yong-SeokKim, Hahn YoungCho, Hyun-JiPark, Jeong WookMoon, Won-JinBae, Hee-Joon
Issue Date
Mar-2023
Publisher
Elsevier BV
Keywords
Vascular cognitive impairment; Stroke; Oxiracetam; Exercise; Functional MRI; Clinical trial
Citation
Contemporary Clinical Trials, v.126
Indexed
SCIE
SCOPUS
Journal Title
Contemporary Clinical Trials
Volume
126
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/62599
DOI
10.1016/j.cct.2023.107108
ISSN
1551-7144
1559-2030
Abstract
Background Oxiracetam may have a modest effect on preventing cognitive decline. Exercise can also enhance cognitive function. This trial aims to investigate the effect of oxiracetam on post-stroke cognitive impairment and explore whether this effect is modified by exercise. Furthermore, the mechanisms that mediate this effect will be investigated through a neural network analysis. Methods This is a multicenter, randomized, double-blind, placebo-controlled phase IV trial. Patients who complained of cognitive decline 3 months after stroke and had a high risk of cognitive decline were eligible. Patients were randomly assigned to receive either 800 mg of oxiracetam or placebo twice daily for 36 weeks. After randomization, a predetermined exercise protocol was provided to each participant, and the degree of physical activity was assessed using wrist actigraphy at 4, 12, 24, and 36 weeks. Resting-state functional MRI was obtained in baseline and 36-week follow-up. Co-primary endpoints are changes in the Mini-Mental State Examination and Clinical Dementia Rating-Sum of Boxes. Secondary endpoints include changes in the NINDS-CSN VCIHS-Neuropsychology Protocol, Euro QoL, patient's global assessment, and functional network connectivity. If there is a significant difference in physical activity between the two groups, the interaction effect between physical activity and the treatment group will be examined. A total of 500 patients were enrolled from February 2018, and the last patient's final follow-up was completed in September 2022. Conclusion This trial is meaningful not only to prove the efficacy of oxiracetam, but also evaluate whether exercise can modify the effects of medication and how cognitive function can be restored. Trial registration http://cris.nih.go.kr (KCT0005137).
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