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To Study the Efficacy of Bromocriptine in Patients With Hepatic/Cirrhosis Related Parkinsonism

A Randomized Open Labelled Placebo Controlled Trial to Study the Efficacy of Bromocriptine in Patients With Hepatic/Cirrhosis Related Parkinsonism

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02265484
Enrollment
50
Registered
2014-10-16
Start date
2013-11-30
Completion date
2015-01-31
Last updated
2016-11-22

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

Conditions

Cirrhosis Related Parkinsonism

Brief summary

After successful screening of liver cirrhosis patients attending ILBS OPD for signs of parkinsonism ( tremor, rigidity or bradykinesia, any 2 of 3). Diagnosis of hepatic/cirrhosis related parkinsonism will be made. Patients will be randomized into Bromocriptine and Placebo. Patients will be followed up every month in OPD (Out Patient Department), ILBS (Institute of liver & Biliary Sciences) for 3 months. Detailed neurological examination will be done at each visit & UPDRS (Unified Parkinson's Disease Rating Scale ) score will be calculated.

Interventions

DRUGLactulose+Rifaximin +Bromocriptine

Sponsors

Institute of Liver and Biliary Sciences, India
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with cirrhosis of liver with signs of parkinsonisms * Patients consented for the study protocol by signing the informed consent.

Exclusion criteria

* Age \< 18 years. * Patient s with HCC (Hepatocellular Carcinoma). * Patients diagnosed as Wilsons disease. * Patient who withdrew or non complaint to the study protocol. * ALF (Acute Liver failure) * Classical Parkinsonism * Atypical Parkinsonism * Pregnancy * Hypotension * Uncontrolled hypertension * CAD * Psychiatric illness * Acute episode of Hepatic encephlopathy

Design outcomes

Primary

MeasureTime frame
The primary outcome will be decrement in UPDRS (Unified Parkinson's Disease Rating Scale) score by 30 %.3 months

Secondary

MeasureTime frame
The secondary end point will be decrement in UPDRS (Unified Parkinson's Disease Rating Scale) score of 10% to 30%.3 months

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026