Add-On Pramipexole for the Treatment of Schizophrenia and Schizoaffective Disorder: A Randomized Controlled Trial

被引:0
|
作者
Levi, Linda [1 ]
Zamora, Daisy [2 ]
Nastas, Igor [3 ]
Gonen, Ilan [4 ]
Radu, Paull [4 ]
Matei, Valentin [5 ]
Ciobanu, Adela M. [5 ]
Nacu, Anatol [3 ]
Boronin, Larisa [3 ]
Karakrah, Lusian [1 ]
Davidson, Michael [6 ]
Davis, John M. [7 ]
Weiser, Mark [1 ,8 ]
机构
[1] Sheba Med Ctr, Dept Psychiat, IL-52621 Tel Hashomer, Israel
[2] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27515 USA
[3] State Univ Med & Pharm Nicolae Testemitanu, Dept Psychiat Narcol & Med Psychol, Kishinev, Moldova
[4] Tangent Alzheimer Care, Breaza, Romania
[5] Univ Med & Pharm Carol Davila, Dept Neurosci, Discipline Psychiat, Bucharest, Romania
[6] Nicosia Univ, Sch Med, Nicosia, Cyprus
[7] Univ Illinois, Dept Psychiat, Chicago, IL 60612 USA
[8] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel
关键词
PLACEBO-CONTROLLED TRIAL; RATING-SCALE; DOUBLE-BLIND; DOPAMINE; PSYCHOSIS; DRUGS;
D O I
10.4088/JCP.21m14233
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: Several small clinical trials have reported that the dopamine agonist pramipexole was beneficial in treating patients with schizophrenia. A confirmatory trial was conducted to test this hypothesis. Methods: This 16-week, multicenter, double-blind, randomized, placebo-controlled study included 200 subjects meeting DSM-IV-TR criteria for schizophrenia or schizoaffective disorder. Patients were randomized to receive either pramipexole (0.75 mg twice daily, n = 100) or placebo (n = 100) as an add-on to their regular antipsychotic treatment. The primary outcome measure was the total score on the Positive and Negative Syndrome Scale (PANSS); secondary outcome measures included PANSS subscale and cognitive functioning scores. Recruitment was performed in 30 sites in Romania and 1 site in the Republic of Moldova between January and June 2011. Results: Analysis of covariance models showed no significant difference between pramipexole and placebo for total PANSS (P> .99) and PANSS positive (P> .99), negative (P= .73), and general psychopathology (P= .99) subscale scores. Changes in Clinical Global Impressions–Severity of Illness scale and Brief Assessment of Cognition in Schizophrenia scores showed no significant difference between pramipexole and placebo. Conclusions: The results of this large randomized controlled trial indicated that pramipexole was not efficacious as an add-on to antipsychotic medications for schizophrenia. © 2022 Physicians Postgraduate Press, Inc.
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页码:47 / +
页数:14
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