Nocturnal Hypertension and Nocturia in African American Men

A Pilot Study : Nocturnal Hypertension and Nocturia in African American Men

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03048734

Enrollment

Registered

2017-02-09

Start date

2017-01-31

Completion date

2017-10-31

Last updated

2020-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Brief summary

This study to obtain pilot data on Nocturnal Hypertension and Nocturia. In Dr. Victor's current NIH grant (Cut Your Pressure Too: The LA Barbershop Blood Pressure Study) the results show that uncontrolled systolic hypertension is independent determinantal of nocturia in African American men. We now went to pursue this correlation by designing a new NIH grant Proposal to determine whether replacing short acting with long acting drugs and dosing them at bed time rather than in the morning will: A. Lower the systolic Blood pressure during sleep B. Improve Nocturia and results in better sleep quality. The results suggest that short acting hydrochlorothiazide may contribute to nocturia in some patients.

Detailed description

AIMS AND SIGNIFICANCE OF PILOT DATA Determine: 1. The feasibility of Southern California registry as an effective measure to recruit African American men to participate in a new research program. 2. If men will comply with the study procedures including Actigraphy and ambulatory blood pressure monitors. 3. The within subject coefficient of variation for repeated measures of nocturnal blood pressure by ambulatory blood pressure monitoring, vertical activity at night by Actigraphy monitors. 4. Whether the ambulatory Blood pressure itself affects the sleep pattern on Actigraphy. 5. Nocturnal systolic blood pressure and nocturnal vertical activity are higher in men with self-reported nocturia ≥2 at night than in men with no reported nocturia. Purpose: Obtain key pilot data to show feasibility and document the reproducibility of the proposed measurements.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

MALE

Age

35 Years to 79 Years

Healthy volunteers

Inclusion criteria

* African American Men * Age 35 to 79 year-old * Able to give informed consent * Pass the home sleep study * Willing to wear the wrist Actigraphy monitor for 9 days continuously. * Willing to wear ambulatory blood pressure monitoring (ABPM) for 48 hours twice during the 9 days of the study period.

Exclusion criteria

* Diabetes Mellitus * Taking Prostate medication * Symptoms of prostate disease or urinary urgency * Sleep apnea 1. A neck circumference greater than 17 inches 2. Using Continuous Positive Airway Pressure (CPAP) 3. History of a diagnosis of Sleep Apnea 4. Apnea Hypopnea Index (AHI) \> 15 per hour

Design outcomes

Primary

Measure	Time frame	Description
Number of events of Nocturia in relation to blood pressure.	9 days	will evaluate the patients with how many times they go to the bathroom and assess the relation with their nocturnal blood pressure.

Outcome results