Clinical Trials Directory

Trials / Completed

CompletedNCT01223391

Abdominal Compression in Orthostatic Hypotension

The Efficacy of Adjustable Lower Abdominal Compression in Neurogenic Orthostatic Hypotension

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess if abdominal binders that use pull strings to adjust compression (non-elastic) are more effective than standard elastic abdominal binders in attenuating neurogenic orthostatic hypotension.

Detailed description

In 3 protocols, patients will undergo standing maneuvers, measured abdominal compressions, continuous BP monitoring and symptoms, ease-of-use and compliance scoring. In protocol 1, patients will exert abdominal compression to maximal tolerable and comfortable levels and values will be recorded. In protocol 2, patients will perform 3 standing maneuvers following a preceding rest period with and without abdominal compression at 20 mmHg (binders used in random order). In protocol 3, the standing maneuvers will be extended and the investigator will adjust binders to levels of abdominal compression corresponding to what patient gauged as maximal tolerable and comfortable levels. Comparison of outcome measures will establish which binder achieves higher abdominal compression, is easier to adjust, likely will be used in the future, if elastic and adjustable binders are equally effective in attenuating Orthostatic Hypotension and its associated symptoms at comparable pressures and which binder is more effective in recovering standing BP and improving orthostatic symptoms.

Conditions

Interventions

TypeNameDescription
OTHERAbdominal binderExternal abdominal compression sequentially applied at 20 mmHg for 3 minutes, maximal tolerable level for 1.5 minutes and comfortable level for 2 minutes.
OTHERNo abdominal binderStanding without abdominal binder for 3 minutes

Timeline

Start date
2010-10-01
Primary completion
2012-08-01
Completion
2012-08-01
First posted
2010-10-19
Last updated
2014-05-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01223391. Inclusion in this directory is not an endorsement.