Skip to content

Assessment of response to levodopa in persons with spinocerebellar ataxia 12 with clinical parkinsonism

Assessment of response to levodopa in persons with spinocerebellar ataxia 12 with clinical parkinsonism - a single arm interventional study - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097282
Enrollment
30
Registered
2025-11-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G258- Other specified extrapyramidal andmovement disorders

Interventions

Intervention1: Tab Levodopa 125 mg TDS: Tablet Levodopa 125 mg will be started and will be hiked to the desired dose of 125 mg TDS in 10 day. Control Intervention1: Nil: Nil

Sponsors

AIIMS New delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: •All adult patients with genetically proven diagnosis of SCA 12 •Presence of clinical features of parkinsonism, as assessed and agreed upon by two movement disorder experts, according to the UK Brain Bank criteria for diagnosis of parkinsonism •Patients on a stable dose of symptomatic medication (e.g. beta-blockers for tremor) for three months prior to enrolment

Exclusion criteria

Exclusion criteria: Participants meeting any one of the following will be excluded . 1.Patients with history of use of any antipsychotic medications, or drugs that can cause drug-induced parkinsonism like D2-blockers etc. in the past 2.Pregnant and lactating females 3.Chronic diseases like Chronic Kidney Disease, Chronic Liver Disease 4.Known allergies or intolerance to levodopa therapy 5.Patients already on levodopa therapy at the time of recruitment 6.Patients who are unwilling to participate

Design outcomes

Primary

MeasureTime frame
change in MDS UPDRS part III score from baseline at three months of levodopa therapy among patients with genetically proven Spino cerebellar ataxia 12 with clinical parkinsonism.Timepoint: baseline and at three months

Secondary

MeasureTime frame
Striatal outcomes using DAT scan in persons with SCA 12Timepoint: at baseline;To assess improvement from baseline in Quality of life using SF 36 , Tremors(tetras score), Non motor symptoms scoreTimepoint: at baseline and 3 months;Correlation between CAG trinucleotide repeats and Levodopa responseTimepoint: at baseline and at 3 months

Countries

India

Contacts

Public ContactDr Lekshmi S H

AIIMS New delhi

achalsrivastava@hotmail.com9811178784

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026