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
| Type | Name | Description |
|---|---|---|
| OTHER | Abdominal binder | External abdominal compression sequentially applied at 20 mmHg for 3 minutes, maximal tolerable level for 1.5 minutes and comfortable level for 2 minutes. |
| OTHER | No abdominal binder | Standing 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.