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A Multicentre, Randomised, Open-Label, Prospective Study to Estimate the Add-On Effects Of Memantine as Ebixa® Oral Pump (Solution) on Language in Patients with Moderate to Severe Alzheimer's Disease Already Receiving Donepezil (ROMEO-AD).
Kim, Hee-Jin; Shim, YongSoo; Han, Hyun Jeong; Kim, Byeong C; Park, Kee Hyung; Moon, So Young; Choi, Seong Hye; Yang, Dong Won; Yoon, Bora; Kim, Eun-Joo; Jeong, Jee Hyang; Han, Seol-Heui.
Afiliação
  • Kim HJ; Department of Neurology, College of Medicine, Hanyang University, Seoul, South Korea. hyumcbrain@hanyang.ac.kr.
  • Shim Y; Department of Neurology, The Catholic University of Korea Eunpyeong St. Mary's Hospital, Seoul, Republic of Korea.
  • Han HJ; Department of Neurology, Myongji Hospital, Hanyang University College of Medicine, Goyang, Republic of Korea.
  • Kim BC; Department of Neurology, Chonnam National University Medical School, Gwangju, Republic of Korea.
  • Park KH; Department of Neurology, College of Medicine, Gil Medical Center, Gachon University, Incheon, Republic of Korea.
  • Moon SY; Department of Neurology, Ajou University School of Medicine, Suwon, Republic of Korea.
  • Choi SH; Department of Neurology, Inha University School of Medicine, Incheon, Republic of Korea.
  • Yang DW; Department of Neurology, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, Republic of Korea.
  • Yoon B; Department of Neurology, Konyang University College of Medicine, Daejeon, Republic of Korea.
  • Kim EJ; Department of Neurology, School of Medicine and Medical Research Institute, Pusan National University Hospital, Pusan National University, Busan, Korea.
  • Jeong JH; Department of Neurology, Ewha Womans University Seoul Hospital, Seoul, Korea.
  • Han SH; Department of Neurology, KonKuk University Seoul Hospital, Seoul, South Korea. alzdoc@kuh.ac.kr.
Neurol Ther ; 12(4): 1221-1233, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37245175
ABSTRACT

INTRODUCTION:

This multicentre, randomised, open-label, and prospective study aimed to evaluate the effectiveness of memantine (memantine solution) on speech function in patients with moderate to severe Alzheimer's disease (AD) who were already on donepezil therapy.

METHODS:

Participants were divided into two groups the drug trial group was administered donepezil + memantine (memantine solution), while the control group was administered only donepezil. Patients in the test group were required to increase the dose of memantine by 5 mg/day per week for the first 4 weeks and were maintained at 20 mg/day until the end of the trial.

RESULTS:

Of the 188 participants, 24 dropped out, and 164 completed the final research process. As the primary outcome, K-WAB showed an increase in scores in both groups compared to baseline scores; however, the difference was not statistically significant (P = 0.678). After 12 weeks, the donepezil treatment group had higher K-MMSE and lower CDR-SB scores than the donepezil and memantine combination group, indicating better cognitive and functional status. However, this effect was not sustained for 24 weeks. Patients who were assigned to receive only donepezil had Relevant Outcome Scale for AD (ROSA) scores that were higher by an average of 4.6 points compared to the donepezil and memantine combination group. The NPI-Q index improved compared to baseline values in both groups.

CONCLUSIONS:

Although several clinical studies have reported significant improvements in speech function after the administration of memantine, clinical studies on speech function improvement in patients with Alzheimer's disease are still insignificant. There are no studies on the effect of donepezil and memantine in combination treatment on language function in the moderate and severe stages of AD. Therefore, we investigated the effect of memantine (memantine solution) on speech function in patients with moderate to severe AD who were administered donepezil at a stable dose. Although the efficacy of the combination therapy was not superior to that of donepezil monotherapy alone, memantine was effective in improving behavioural symptoms in patients with moderate or severe AD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies Idioma: En Revista: Neurol Ther Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies Idioma: En Revista: Neurol Ther Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Coréia do Sul