Water and the Gastropressor Response - Diurnal Variability
This study is ongoing, but not recruiting participants.
Sponsor:
Satish R. Raj
Information provided by (Responsible Party):
Satish R. Raj, Vanderbilt University
ClinicalTrials.gov Identifier:
NCT00581373
First received: December 22, 2007
Last updated: January 7, 2013
Last verified: January 2013
| Tracking Information | |||||
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| First Received Date ICMJE | December 22, 2007 | ||||
| Last Updated Date | January 7, 2013 | ||||
| Start Date ICMJE | August 2007 | ||||
| Estimated Primary Completion Date | December 2014 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
blood pressure [ Time Frame: 1 day ] [ Designated as safety issue: No ] | ||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT00581373 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
heart rate [ Time Frame: 1 day ] [ Designated as safety issue: No ] | ||||
| Original Secondary Outcome Measures ICMJE | Same as current | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Water and the Gastropressor Response - Diurnal Variability | ||||
| Official Title ICMJE | Water and the Gastropressor Response - Diurnal Variability (Specific Aim 1.3) | ||||
| Brief Summary | We will test the null hypothesis that there is no diurnal (morning to afternoon)variability in the blood pressure response to the ingestion of water 16 oz. |
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| Detailed Description | Not Provided | ||||
| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
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| Condition ICMJE | Orthostatic Hypotension | ||||
| Intervention ICMJE | Other: water 16 fl oz
water 16 fl oz in AM and repeat in late afternoon |
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| Study Arm (s) | Experimental: 1
water 16 oz
Intervention: Other: water 16 fl oz |
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| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Active, not recruiting | ||||
| Estimated Enrollment ICMJE | 20 | ||||
| Estimated Completion Date | December 2014 | ||||
| Estimated Primary Completion Date | December 2014 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years to 80 Years | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00581373 | ||||
| Other Study ID Numbers ICMJE | 060553, Vanderbilt Discovery | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Satish R. Raj, Vanderbilt University | ||||
| Study Sponsor ICMJE | Satish R. Raj | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Vanderbilt University | ||||
| Verification Date | January 2013 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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