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Insomnia Prevalence and Treatment Impact on Systemic Hypertension

Insomnia Prevalence and Treatment Impact on Systemic Hypertension

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05414864
Acronym
Print-HAS
Enrollment
5
Registered
2022-06-10
Start date
2022-05-01
Completion date
2022-09-30
Last updated
2022-12-29

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

Conditions

Hypertension, Insomnia

Keywords

insomnia, hypertension, Ramelteon, sleep hygiene

Brief summary

Insomnia is defined as some difficulty in sleep onset, consolidation, duration, or quality, despite appropriate opportunities for getting sleep. In the last decade, there is growing evidence associating insomnia and high blood pressure, (HBP), coronary disease, heart failure, atrial fibrillation, as well as with an increased mortality rate. Despite the previously mentioned advances, the real impact of insomnia on HBP is unknown. It is unclear whether the diagnosis and pharmacologic treatment of insomnia will have an impact on 24-h BP. The aim of this study is to outline the prevalence of insomnia in patients with HBP followed in the ambulatories from the Hypertension Units at InCor and Hospital das Clínicas. The main hypothesis is that the prevalence of insomnia is high and most patients remain undiagnosed and consequently untreated. For this phase, up to 1,500 patients with HBP will be selected. Besides the medical records with demographic and anthropometric data, personal and familiar background, as well as regular medication, all patients will perform three systematic and standardized blood pressure checks on electric monitors.

Detailed description

Prevalence of insomnia in patients with HBP The aim of this study is to outline the prevalence of insomnia in patients with HBP followed by the outpatients' clinics at the InCor and Hospital das Clínicas. The main hypothesis is that the prevalence of insomnia is high and most patients remain undiagnosed and consequently untreated. For this phase, up to 1,500 patients with HBP will be recruited. Besides the medical records with demographic and anthropometric data, personal and familiar background, as well as regular medication, all patients will perform three systematic and standardized blood pressure checks on electric monitors. The average of the second and third checks will be the final result. Furthermore, the following exams will be made: 1. Definition of the presence of insomnia following the criteria from DSM V and filling up the insomnia severity index. 2. Evaluation of the Pittsburgh Sleep Quality Index. 3. Evaluation of obstructive sleep apnea by NoSAS score. 4. Evaluation of daytime sleepiness by the Epworth Sleepiness Scale. 5. Filling the DDAS form for evaluation of perception and impact of insomnia on the life of HBP patients. 6. Filling the Beck form for depression evaluation. The clinical characteristics of HBP patients with and without insomnia will be compared testing the hypothesis that patients with insomnia will be under more blood pressure medications and/or uncontrolled bllod pressure than patients without insomnia. If positive, a multivariate analysis will be performed for adjusting for counfonding factors.

Interventions

DRUGRamelteon (RozeremR)

8mg daily

BEHAVIORALsleep hygiene

sleep behavioral guidelines

Sponsors

Takeda
CollaboratorINDUSTRY
University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Masking description

team that evaluate the results of complementary exams

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* BMI \<40Kg/m2; * Availability to participate * History of HBP under regular treatment (systolic pressure between 130-160 and diastolic pressure between 80-100 mmHg).

Exclusion criteria

* Use of benzodiazepines or Z drugs; * Night workers; * History of severe chronic obstructive pulmonary disease (COPD); * Heart failure (ejection fraction \<40% on echocardiogram); * Prior stroke; * Generalized anxiety disorder (GAD-7 \>14 points) and severe depression (Beck); * Severe liver disease; * Alcohol abuse; * Advanced chronic kidney disease 4 or 5 (glomerular filtration rate \<30ml/min/1.73m2); * Patient who is on loop diuretics; * Patient with type 1 diabetes; * Patient with decompensated type 2 diabetes (Glycated hemoglobin \>8%); * Urinuria Incontinence; * Prostatism; * History of active cancer; * Pregnancy; * Complex sleep behaviors, suicidal behavior; * Other formal labeled contraindications, including a history of angioedema with ramelteone and patients using fluvoxamine (a strong inhibitor of CYP1A2)

Design outcomes

Primary

MeasureTime frameDescription
Efficacy of insomnia treatment on blood pressure (evaluated by Ambulatory blood pressure monitoring)3 monthsTo assess the impact of treatment of early insomnia with ramelteon on daytime and nighttime blood presure (in mmHg) in hypertensive patients on 24-hour evaluation of ambulatory blood pressure monitoring.

Secondary

MeasureTime frameDescription
Efficacy of insomnia treatment on blood pressure (evaluated by office blood pressure)3 monthsTo evaluate the impact of treating initial insomnia with ramelteone on office blood pressure in hypertensive patients on office blood pressure (in mmHg)
Efficacy of insomnia treatment on Sleep duration3 monthsTo assess the impact of treating insomnia with ramelteon in hypertensive patients on sleep duration evaluated by actigraphy (and reported in minutes of sleep);
Efficacy of insomnia treatment on sleep quality3 monthsTo evaluate the impact of treating insomnia with ramelteon in hypertensive patients on sleep quality;
Efficacy of insomnia treatment on subgroups of patients (intending to be a sub-study)3 monthsAssess whether the pressure response of insomnia treatment on the primary and secondary outcomes is mediated by the presence of obstructive sleep apnea.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026