Observational studyMovement disorders clinical practice2026
Levodopa-Carbidopa Intestinal Gel Improves Dyskinesia in Parkinson's Disease: Post Hoc Analysis from the COSMOS Study.
Observational study in Movement disorders clinical practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03362879 (COSMOS - COmedication Study Assessing Mono- and cOmbination Therapy With Levodopa-carbidopa inteStinal Gel), which is not on this map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
COSMOS - COmedication Study Assessing Mono- and cOmbination Therapy With Levodopa-carbidopa inteStinal Gel
Who cites it
3 citing papers in PubMed.
- Long-Term Clinical Efficacy, Safety, and Polypharmacy Simplification of Levodopa-Entacapone-Carbidopa Intestinal Gel in Advanced Parkinson's Disease: An 18-Month Longitudinal Study.Journal of clinical medicine · 2026Article
- Clinical Outcomes and Predictors of Response to Levodopa-Entacapone-Carbidopa Intestinal Gel in Advanced Parkinson's Disease: A Retrospective Cohort Study over a 4-Year Period.Pharmaceutics · 2026Article
- L-Dopa/Carbidopa intestinal gel infusion in advanced Parkinson's disease: real-life mobility insights from wearable sensors.Frontiers in neurologyArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
Abstract
backgroundDyskinesia is a debilitating complication of dopaminergic therapy in advanced Parkinson's disease.
objectivesTo evaluate the effect of levodopa-carbidopa intestinal gel (LCIG) on dyskinesia burden.
methodsThis is a post hoc analysis of the retrospective, observational COmedication Study assessing Mono- and cOmbination therapy with levodopa-carbidopa inteStinal gel (COSMOS; NCT03362879). Change in dyskinesia was assessed by LCIG treatment group (monotherapy, daytime monotherapy, polytherapy), baseline dyskinesia duration (<4 vs. ≥4 hours), and dyskinesia severity (troublesome vs. non-troublesome). Correlations between changes in dyskinesia and patient-reported outcomes (Parkinson's Disease Questionnaire-8 [PDQ-8], Parkinson's Disease Sleep Scale-2 [PDSS-2], non-motor symptoms scale [NMSS]) were assessed using Spearman correlation coefficients. The Unified Parkinson's Disease Rating Scale IV measured dyskinesia duration (Item 32), severity (Item 33), and pain (Item 34). Data were collected cross-sectionally at a single study visit.
resultsOver 50% (202/369) of LCIG-treated patients experienced improvement in dyskinesia severity. Improvements in dyskinesia duration and severity were noted in all treatment groups. The proportion of patients with troublesome dyskinesia and amount of "Off" time significantly decreased from baseline to study visit, regardless of baseline dyskinesia burden (P < 0.01); dyskinesia duration improved only in the ≥4-hour subgroup (P < 0.01). In the ≥4-hour subgroup, dyskinesia duration correlated positively with PDQ-8; dyskinesia severity correlated positively with PDQ-8 and PDSS-2; and dyskinesia pain correlated positively with PDQ-8, PDSS-2, and NMSS.
conclusionLCIG led to reductions in dyskinesia severity, regardless of baseline dyskinesia burden. Dyskinesia duration improved in patients with high dyskinesia burden but not in those with low dyskinesia burden.
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