drugset / Trial / NCT02265484

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

NCT02265484 ↗

RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2013-11
Primary completion
2015-01
Completion
2015-01

Outcome

Met primary endpoint

paper Bromocriptine therapy for 12 weeks resulted in improvement in rigidity, tremors, bradykinesia and gait compared to placebo PMID 30554466 ↗

paper complete and partial response in seven vs none (29.1%, 0%, P < 0.01) and 12 vs one (50%, 4.5%, P < 0.01) patients. PMID 30554466 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bromocriptine Small molecule — —
Background Lactulose Other / unclassified — —
Background Rifaximin Other / unclassified — —

Indications