General information
  • Disease category Nervous System diseases (BASEC)
  • Study Phase Phase 1/Phase 2 (ICTRP)
  • Recruitment status recruitment not started yet (BASEC/ICTRP)
  • Trial sites
    Lausanne
    (BASEC)
  • Contact Dr Julien Bally julien.bally@chuv.ch (BASEC)
  • Data Source(s) BASEC: Import from 02.04.2025 ICTRP: Import from 20.03.2025
  • Last update 02.04.2025 08:21
HumRes66384 | SNCTP000006280 | BASEC2024-02568 | NCT06831500

Monocentric, randomized, double-blind study to evaluate the feasibility of conducting a large-scale clinical trial aimed at measuring the effect of the Carbidopa/Levodopa ratio on orthostatic hypotension (OH) in patients with multiple system atrophy – parkinsonian form (MSA-P) or Parkinson's disease (PD). (CARBIDOH)

  • Disease category Nervous System diseases (BASEC)
  • Study Phase Phase 1/Phase 2 (ICTRP)
  • Recruitment status recruitment not started yet (BASEC/ICTRP)
  • Trial sites
    Lausanne
    (BASEC)
  • Contact Dr Julien Bally julien.bally@chuv.ch (BASEC)
  • Data Source(s) BASEC: Import from 02.04.2025 ICTRP: Import from 20.03.2025
  • Last update 02.04.2025 08:21

Summary description of the study

This study is aimed at patients with multiple system atrophy – parkinsonian form – (MSA-P) or Parkinson's disease (PD), receiving dopaminergic medications and suffering from orthostatic hypotension (OH). OH is a drop in blood pressure upon standing that can lead to symptoms of dizziness, lightheadedness, blackouts, and can, when severe, lead to fainting. OH is part of the symptoms present in MSA-P and PD. The standard treatment for parkinsonian symptoms such as slowness and stiffness consists of administering antiparkinsonian medications containing dopamine. These dopaminergic medications always contain 1) levodopa (which is the precursor of dopamine) and 2) an enzyme inhibitor, which can 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 medications worsen OH. Through various mechanisms, this worsening of OH is related to both levodopa and the enzyme inhibitor with which it is combined. However, we do not know the respective effects of these two molecules on OH. In this study, we examine how, through the different dosages of the dopaminergic medication under investigation, the Carbidopa/Levodopa ratio affects OH.

(BASEC)

Intervention under investigation

Participants will receive, once a week, in a predetermined random order, and without either they or the study physician knowing the ratio administered at each visit, the 3 different ratios of carbidopa/levodopa, the medication under study:

- 1:2 (100 mg of carbidopa / 200 mg of levodopa) or

- 1:4 (50 mg of carbidopa / 200 mg of levodopa) or

- 1:10 (20 mg of carbidopa / 200 mg of levodopa).

An orthostatic test (measurement of orthostatic hypotension when transitioning from lying down to standing) as well as an evaluation of motor symptoms will be carried out before and after taking each dosage of Carbidopa/Levodopa, the dopaminergic medication under investigation.

(BASEC)

Disease under investigation

Orthostatic hypotension (OH) in patients with multiple system atrophy – parkinsonian form (MSA-P) or Parkinson's disease (PD).

(BASEC)

Criteria for participation in trial
- Patient aged over 18 years and under 80 years. - Patient with multiple system atrophy of parkinsonian type or Parkinson's disease presenting symptoms of orthostatic hypotension. - Patient currently receiving dopaminergic treatment (Levodopa combined with Carbidopa or Benserazide). (BASEC)

Exclusion criteria
- Patient unable to tolerate a one-night (at least 12 hours) interruption of their immediate-release dopaminergic treatment (and at least 24 hours if extended, delayed, or controlled release). - Patient with dementia (i.e., major cognitive impairment) associated with MSA-P or PD, - Patient with mild cognitive impairment and unable to fully give or understand informed consent, i.e., who does not have full discernment capacity. - Patient with known congestive heart failure, grades C and D, NYHA III and IV. - Current participation in other clinical trials. - Pregnant or breastfeeding woman or wishing to become pregnant. (BASEC)

Trial sites

Lausanne

(BASEC)

Switzerland (ICTRP)

Sponsor

Sponsor: Centre Hospitalier Universitaire Vaudois (CHUV) Sponsor's representative: Dr Julien F. Bally, PD-MER Head of the Movement Disorder Unit Department of Clinical Neurosciences Service of Neurology Centre Hospitalier Universitaire Vaudois (CHUV) Rue du Bugnon 46, 1011 Lausanne, Switzerland

(BASEC)

Contact

Contact Person Switzerland

Dr Julien Bally

+41 21 314 11 92

julien.bally@chuv.ch

Unité des mouvements anormaux Service de Neurologie Centre Universitaire Hospitalier Vaudois (CHUV) Rue du Bugnon 46 1011 Lausanne

(BASEC)

General Information

+41 79 556 78 19+41 79 556 78 19

julien.bally@chuv.ch

(ICTRP)

Name of the authorising ethics committee (for multicentre studies, only the lead committee)

Ethics Committee Vaud

(BASEC)

Date of authorisation

19.02.2025

(BASEC)


ICTRP Trial ID
NCT06831500 (ICTRP)

Official title (approved by ethics committee)
A monocentric, randomized, double-blind study to assess the feasibility of conducting a full-scale randomized controlled trial (RCT) assessing the effect of carbidopa/levodopa ratio on orthostatic hypotension (OH) in Multiple System Atrophy - Parkinsonian type (MSA-P) and Parkinson Disease (PD) patients. (BASEC)

Academic title
A Monocentric, Randomized, Double-blind Study to Assess the Feasibility of Conducting a Full-scale Randomized Controlled Trial (RCT) Assessing the Effect of Carbidopa/levodopa Ratio on Orthostatic Hypotension (OH) in Multiple System Atrophy - Parkinsonian Type (MSA-P) and Parkinson Disease (PD) Patients (CARBIDOH) (ICTRP)

Public title
Feasibility Study Assessing the Effect of Carbidopa/levodopa Ratio on Orthostatic Hypotension in Multiple System Atrophy - Parkinsonian Type and Parkinson Disease. (ICTRP)

Disease under investigation
Multi-system Atrophy - Parkinsonian TypeOrthostatic Hypotension, DysautonomicParkinson Disease (ICTRP)

Intervention under investigation
Drug: Administration of Carbidopa/levodopa (ICTRP)

Type of trial
Interventional (ICTRP)

Trial design
Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Treatment. Masking: Double (Participant, Investigator). (ICTRP)

Inclusion/Exclusion criteria
Inclusion Criteria:

1. Informed consent form signed.

2. Patient over 18 years and under 80 years of age.

3. Patient with Multiple System Atrophy- Parkinsonian type (MSA-P) (confirmed by
diagnostic criteria for clinically established and clinically probable multiple
system atrophy (11) OR Patient with Parkinson Disease (PD) (12) presenting OH
symptoms (getting at least one point at the 3 questions - n 14, 15 and 16 - of the
SCOPA-AUT scale that address orthostatic hypotension symptoms).

4. Patient currently receiving Dopamine-Replacement Therapy (i.e. Levodopa combined
with Carbidopa or Benserazide).

Exclusion Criteria:

1. Patient unable to stand an overnight (at least 12 hours) withdrawal of their
immediate-release DRT (last extended-, delayed-, or controlled-release dosage must
be taken minimum 24 hours prior to the test).

2. Patient with known congestive heart failure, grades C and D, NYHA III and IV.

3. Patient with dementia (i.e. major cognitive impairment) associated to MSA-P or PD,

4. Patient with mild cognitive impairment, and unable to provide or understand informed
consent, i.e. who does not have full capacity for discernment.

5. Current participation to other clinical trials.

6. Pregnant or lactating woman or willing to become pregnant. (ICTRP)

not available

Primary and secondary end points
Feasibility of future large-scale double-blind randomized controlled trial (RCT) (ICTRP)

not available

Registration date
not available

Incorporation of the first participant
not available

Secondary sponsors
not available

Additional contacts
Julien BALLY, Dr PD-MERJulien Bally, Dr. PD MER, julien.bally@chuv.chjulien.bally@chuv.ch, +41 79 556 78 19+41 79 556 78 19 (ICTRP)

Secondary trial IDs
2024-02568 (ICTRP)

Results-Individual Participant Data (IPD)
not available

Further information on the trial
https://clinicaltrials.gov/ct2/show/NCT06831500 (ICTRP)

Results of the trial

Results summary

not available

Link to the results in the primary register

not available