Page last updated: 2024-11-04

ropinirole and Hallucinations

ropinirole has been researched along with Hallucinations in 5 studies

Hallucinations: Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS.

Research Excerpts

ExcerptRelevanceReference
"Ropinirole XL/PR was titrated/continued, and adjusted as appropriate during the maintenance phase (maximum 24 mg/d)."2.82Long-term, open-label, safety study of once-daily ropinirole extended/prolonged release in early and advanced Parkinson's disease. ( Asgharian, A; Ellis, J; Jimenez, T; Makumi, CW; Shaikh, S; VanMeter, S, 2016)
" In the group of patients with prior dopamine-agonist therapy, more patients reported adverse events in the ropinirole group (90% versus 79%, p < 0."2.70A six-month multicentre, double-blind, bromocriptine-controlled study of the safety and efficacy of ropinirole in the treatment of patients with Parkinson's disease not optimally controlled by L-dopa. ( Brooks, DJ; Brunt, ER; Korczyn, AD; Montastruc, JL; Stocchi, F, 2002)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (60.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Makumi, CW1
Asgharian, A1
Ellis, J1
Shaikh, S1
Jimenez, T1
VanMeter, S1
Nissen, T1
Newman, EJ1
Grosset, KA1
Daghem, M1
Pal, G1
Stewart, M1
Odin, P1
Macphee, GJ1
Grosset, DG1
Pae, CU1
Marks, DM1
Han, C1
Patkar, AA1
Yamamoto, T1
Brunt, ER1
Brooks, DJ1
Korczyn, AD1
Montastruc, JL1
Stocchi, F1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
An Open-Label Extension Study With REQUIP (Ropinirole) CR for Subjects From Studies 101468/165, 101468/168 and 101468/169[NCT00632736]Phase 3419 participants (Actual)Interventional2004-02-29Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Number of Participants With the Indicated Number of Adverse Events (AEs) and Serious Adverse Events (SAEs)

AEs, defined as any unfavorable and unintended sign, symptom, or disease temporally associated with the use of a medicinal product, were collected to obtain data on the safety, tolerability, and benefit of ropinirole XL. SAEs, defined as AEs that are fatal, life threatening, disabling/incapacitating, resulting in hospitalization or prolongation of a hospital stay, a congenital abnormality/birth defect, or any important medical occurrence that the investigator regards as serious based on medical judgment, were also collected. st. med., study medication. (NCT00632736)
Timeframe: 13 February 2004 through 31 March 2010

Interventionparticipants (Number)
Participants (Par.) reporting at least one AEPar. reporting at least one SAEPar. with drug-related AEsPar. with AEs leading to withdrawal
Ropinirole XL365109213106

Number of Participants With the Indicated Response to the Patient Preference Question at Week 4 and Week 26

"The patient preference question assessed the participant's preference for either dosing regimen of study drug, once a day versus three times a day. Participants were asked to respond to the following question to assess preference: Please indicate whether you preferred taking your Parkinson's tablets 3 times a day or once a day. Wk, Week." (NCT00632736)
Timeframe: Week 4 and Week 26

Interventionparticipants (Number)
Very much preferred three times a day, Wk 4, n=74Much preferred three times a day, Week 4, n=74Preferred three times a day, Week 4, n=74Both regimens are about the same, Week 4, n=74Preferred once a day, Week 4, n=74Much preferred once a day, Week 4, n=74Very much preferred once a day, Week 4, n=74Very much preferred three times a day, Wk 26, n=87Much preferred three times a day, Week 26, n=87Preferred three times a day, Week 26, n=87Both regimens are about the same, Week 26, n=87Preferred once a day, Week 26, n=87Much preferred once a day, Week 26, n=87Very much preferred once a day, Week 26, n=87
Ropinirole XL20451718284124142042

Trials

2 trials available for ropinirole and Hallucinations

ArticleYear
Long-term, open-label, safety study of once-daily ropinirole extended/prolonged release in early and advanced Parkinson's disease.
    The International journal of neuroscience, 2016, Volume: 126, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Antiparkinson Agents; Back Pain; Delayed-Action Preparations; Dopami

2016
A six-month multicentre, double-blind, bromocriptine-controlled study of the safety and efficacy of ropinirole in the treatment of patients with Parkinson's disease not optimally controlled by L-dopa.
    Journal of neural transmission (Vienna, Austria : 1996), 2002, Volume: 109, Issue:4

    Topics: Adult; Aged; Aged, 80 and over; Antiparkinson Agents; Bromocriptine; Double-Blind Method; Drug Thera

2002

Other Studies

3 other studies available for ropinirole and Hallucinations

ArticleYear
Duration of L-dopa and dopamine agonist monotherapy in Parkinson's disease.
    Scottish medical journal, 2012, Volume: 57, Issue:4

    Topics: Aged; Antiparkinson Agents; Benzothiazoles; Confidence Intervals; Disorders of Excessive Somnolence;

2012
A case of transient hallucination with ropinirole augmentation antidepressant in a patient with treatment-resistant depression: Is there differential effect of ropinirole dose on developing psychotic symptom?
    Progress in neuro-psychopharmacology & biological psychiatry, 2008, May-15, Volume: 32, Issue:4

    Topics: Antidepressive Agents; Depressive Disorder; Depressive Disorder, Major; Dopamine Agonists; Drug Resi

2008
Ropinirole as compared with levodopa in Parkinson's disease.
    The New England journal of medicine, 2000, Sep-21, Volume: 343, Issue:12

    Topics: Antiparkinson Agents; Dyskinesia, Drug-Induced; Hallucinations; Humans; Indoles; Levodopa; Parkinson

2000