Condition: Multi-system Atrophy - Parkinsonian Type · Orthostatic Hypotension, Dysautonomic · Parkinson Disease · Sponsor: Julien Bally
This study is aimed at patients with multi-system atrophy - parkinsonian type (P-MSA) or Parkinson's disease (PD) receiving dopaminergic drugs and suffering from orthostatic hypotension (OH). OH is a drop in blood pressure when standing, which can lead to symptoms of dizziness, lightheadedness, a black veil in front of the eyes and, when severe, can lead to fainting. HO is one of the symptoms present in AMS-P and PD. The standard treatment for parkinsonian symptoms of slowness and stiffness is the administration of antiparkinsonian drugs containing dopamine. These dopaminergic drugs always contain 1) levodopa (which is the precursor of dopamine) and 2) an enzyme inhibitor, which may be either benserazide (in the case of Madopar® and its generics) or carbidopa (in the case of Sinemet® or Stalevo® and their generics) and whose role is to potentiate the effect of levodopa. It has long been known that dopaminergic drugs aggravate HO. Through various mechanisms, this worsening of HO is linked as much to levodopa as to the enzyme inhibitor with which it is combined. However, investigators do not know the respective effects of these two molecules on HO. In this study, investigators examine how the ratio of Carbidopa to levodopa affects HO in the various assays of the dopaminergic drug under study.
This description comes directly from the study's public registry record.
Julien BALLY, Dr PD-MER · +41 79 556 78 19 · julien.bally@chuv.ch
Always discuss trial participation with your own doctor first.
| Centre Hospitalier Universitaire Vaudois (CHUV) | Lausanne, Canton of Vaud, Switzerland | Recruiting |
| Centre Hospitalier Universitaire Vaudois | Lausanne, Canton of Vaud, Switzerland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06831500