Blood Pressure Monitor Clinical Test (Cuff Range: 22 Cm-42cm)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT01575067 |
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Recruitment Status :
Completed
First Posted : April 11, 2012
Last Update Posted : April 11, 2012
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Sponsor:
Andon Health Co., Ltd
Information provided by (Responsible Party):
Andon Health Co., Ltd
| Tracking Information | |||
|---|---|---|---|
| First Submitted Date | April 9, 2012 | ||
| First Posted Date | April 11, 2012 | ||
| Last Update Posted Date | April 11, 2012 | ||
| Study Start Date | February 2012 | ||
| Actual Primary Completion Date | April 2012 (Final data collection date for primary outcome measure) | ||
| Current Primary Outcome Measures | Not Provided | ||
| Original Primary Outcome Measures | Not Provided | ||
| Change History | No Changes Posted | ||
| Current Secondary Outcome Measures | Not Provided | ||
| Original Secondary Outcome Measures | Not Provided | ||
| Current Other Pre-specified Outcome Measures | Not Provided | ||
| Original Other Pre-specified Outcome Measures | Not Provided | ||
| Descriptive Information | |||
| Brief Title | Blood Pressure Monitor Clinical Test (Cuff Range: 22 Cm-42cm) | ||
| Official Title | Not Provided | ||
| Brief Summary | The purpose of this study is to monitor the blood pressure level of the patient using a preformed cuff ranged 22 cm-42 cm. | ||
| Detailed Description | Not Provided | ||
| Study Type | Observational | ||
| Study Design | Time Perspective: Prospective | ||
| Target Follow-Up Duration | Not Provided | ||
| Biospecimen | Not Provided | ||
| Sampling Method | Non-Probability Sample | ||
| Study Population | resident of a community | ||
| Condition | Blood Pressure | ||
| Intervention | Not Provided | ||
| Study Groups/Cohorts |
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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 | Completed | ||
| Actual Enrollment |
85 | ||
| Original Actual Enrollment | Same as current | ||
| Actual Study Completion Date | April 2012 | ||
| Actual Primary Completion Date | April 2012 (Final data collection date for primary outcome measure) | ||
| Eligibility Criteria | Inclusion Criteria:
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| Sex/Gender |
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| Ages | 30 Years to 84 Years (Adult, Older Adult) | ||
| Accepts Healthy Volunteers | Yes | ||
| Contacts | Contact information is only displayed when the study is recruiting subjects | ||
| Listed Location Countries | Not Provided | ||
| Removed Location Countries | |||
| Administrative Information | |||
| NCT Number | NCT01575067 | ||
| Other Study ID Numbers | AndonHealth5 | ||
| Has Data Monitoring Committee | No | ||
| U.S. FDA-regulated Product | Not Provided | ||
| IPD Sharing Statement | Not Provided | ||
| Responsible Party | Andon Health Co., Ltd | ||
| Study Sponsor | Andon Health Co., Ltd | ||
| Collaborators | Not Provided | ||
| Investigators | Not Provided | ||
| PRS Account | Andon Health Co., Ltd | ||
| Verification Date | April 2012 | ||