Clinical Trials Directory

Trials / Completed

CompletedNCT00103597

Efficacy of Therapeutic Interventions for Orthostatic Hypotension in Parkinson's Disease and Multiple System Atrophy

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
50 (planned)
Sponsor
Royal Brisbane and Women's Hospital · Other Government
Sex
All
Age
40 Years – 95 Years
Healthy volunteers
Not accepted

Summary

Patients with Parkinson's Disease or Multiple System Atrophy (MSA), and symptoms of orthostatic hypotension, are eligible for the study. Each patient will have three weeks of conservative therapy, three weeks of therapy with fludrocortisone, and three weeks of therapy with domperidone. Autonomic testing, a symptom questionnaire, bedside blood pressure testing, and Unified Parkinson Disease Rating Scale (UPDRS) will be performed after each intervention.

Detailed description

Enrolled patients, ages 40-95, must have Parkinson's or MSA, diagnosed by a neurologist, and symptoms of orthostatic hypotension. Each patient will fill out two validated questionnaires to determine if they are candidates for the study. Baseline patient details, such as their medications and UPDRS, will be recorded. Medications must be held stable during the period of the study. Each patient will then have three weeks of conservative therapy, three weeks of therapy with fludrocortisone, and three weeks of therapy with domperidone. Autonomic testing, a symptom questionnaire, bedside blood pressure testing, and UPDRS will be performed after each intervention.

Conditions

Interventions

TypeNameDescription
DRUGFludrocortisone
DRUGDomperidone
BEHAVIORALConservative Measures for Orthostatic Hypotension

Timeline

Start date
2005-01-01
Completion
2005-09-01
First posted
2005-02-14
Last updated
2005-10-20

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT00103597. Inclusion in this directory is not an endorsement.