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Phase 4 N=9 Other

Lundbeck TOMs Orthostatic Hypotension

Orthostatic Hypotension · Idiopathic Parkinson Disease

Enrolled (actual)
9
Serious AEs
0.0%
Results posted
Sep 2022
Primary outcome: Primary: Orthostatic Hypotension Questionnaire (OHQ) Score — 4.6 score on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Droxidopa 100 MG [Northera] (Drug)
Age
Adult, Older Adult · 30+ yrs
Sex
All
Sponsor
Alberto Espay, MD, MSc
Primary completion
Dec 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Orthostatic Hypotension Questionnaire (OHQ) Score
4.6
PRIMARY
Tinetti Score
13.4
PRIMARY
PDQ-39 Score
31
PRIMARY
Gait Analysis - Stride Length
60.3
PRIMARY
Gait Analysis - Single Leg Stance Time
34.6
PRIMARY
Gait Analysis - Gait Velocity
112.1
PRIMARY
Postural Analysis - Postural Sway
35.8

Summary

Orthostatic hypotension (OH), which consists in a significant reduction in blood pressure levels upon standing from a seated position, may affect approximately one in three patients with Parkinson's disease (PD). It usually presents as dizziness, lightheadedness, feeling faint, or feeling like you might black out while standing. This can significantly impact the quality of life (QoL) of PD patients, resulting in difficulties with balance, walking, and increased risk of falls. The main aim of this study is to evaluate whether the use of technological devices (a computerized system for analyzing abnormalities in walking in clinical settings and a wearable sensor to detect changes in postural unsteadiness in the home environment) may improve the detection of complications and the response to medical therapies for OH in patients with PD.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of idiopathic Parkinson's Disease, meeting UK Brain Bank criteria for at least 3 years
  • Hoehn and Yahr (H&Y) stage I-III
  • Age between 30 and 80 years old (both inclusive)
  • Stable dosage of dopaminergic medications for at least 4 weeks
  • Orthostatic Hypotension, defined as a fall in systolic BP ≥ 20 mmHg or diastolic BP ≥ 10 mmHg within 3 minutes of standing
  • Willingness and ability to comply with scheduled visits

Exclusion Criteria

  • Diabetes mellitus or other diseases potentially associated with autonomic dysfunction
  • Treatment with antihypertensive drugs or with alpha-adrenergic antagonists
  • Cognitive impairment, defined as a score 2 at the MDS-UPDRS item 3.12 (recover at the pull test)
  • Severe levodopa induced dyskinesia, defined as an MDS-UPDRS item 4.2 > 2 (functional impact of dyskinesia)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04510922). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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