Chronotherapy with Low-dose Aspirin for Primary Prevention

NCT ID: NCT00725127

Last Updated: 2024-12-06

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE4
• Total Enrollment: 3200 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-10-31
• Study Completion Date: 2026-06-30

Brief Summary

Brief summary:

Aspirin (ASA) has been shown to provide marked benefits in primary and secondary prevention of cardiovascular events. Substantial evidence suggests that low-dose ASA therapy should also be used as a primary prevention strategy in men and women with diabetes who are at high cardiovascular risk. On the other hand, there is current evidence on the potential benefits of low-dose ASA therapy in subjects with impaired fasting glucose, including those with metabolic syndrome. Most important, previous laboratory animal and clinical trial research convincingly demonstrates administration time-dependent (with reference to circadian rhythms) effects of ASA. Thus, the effects of ASA upon lipoperoxides, b-adrenergic receptors, and blood pressure (BP) in clinically healthy subjects depend on the circadian timing of ASA administration. The administration-time-dependent influence of ASA on BP was previously demonstrated in a randomized trial on healthy women and other independent double-blind, randomized, placebo-controlled clinical trials conducted, first, on clinically healthy subjects, a second one on normotensive and hypertensive subjects, a third one on pregnant women at high risk for preeclampsia and a fourth one in previously untreated patients with mild hypertension. The findings of these BP studies are consistent; BP-lowering effect of low-dose ASA is achieved when administered at bedtime but not upon awakening.

In keeping with the chronopharmacological effects of ASA and the previous findings suggesting that ASA at low dose may exert a potential beneficial effect on BP, endothelium function and cardiovascular function, this prospective, randomized, parallel-arm study will investigate the potential influence of ASA on the primary prevention of cardiovascular, cerebrovascular and renal events in subjects with either impaired fasting glucose (≥ 100 mg/dl) or previous diagnosis of type 2 diabetes mellitus, who will receive low-dose ASA (100 mg/day) at different circadian times (upon awakening or at bedtime) in relation to their rest-activity cycle.

Conditions

Type 2 Diabetes

Keywords

Aspirin; Chronotherapy; Primary prevention; Impaired fasting glucose; Type 2 diabetes; Total mortality; Myocardial infarction; Stroke; Angina pectoris; Chronic kidney disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

1

100 mg/day ASA upon awakening.

Group Type: ACTIVE_COMPARATOR

aspirin

Intervention Type: DRUG

100 mg/day upon awakening for five years

2

100 mg/day ASA at bedtime

Group Type: ACTIVE_COMPARATOR

aspirin

Intervention Type: DRUG

100 mg/day at bedtime for five years

Interventions

aspirin

100 mg/day upon awakening for five years

Intervention Type: DRUG

aspirin

100 mg/day at bedtime for five years

Intervention Type: DRUG

Other Intervention Names

Aspirin on awakening; Aspirin at bedtime

Eligibility Criteria

Inclusion Criteria

• Male or female subjects ≥ 50 years of age.
• Impaired fasting glucose (≥ 100 and < 126 mg/dl) in the last available blood test prior (≤ 3 months) to randomization, or diagnosis of type 2 diabetes prior to randomization.
• All subjects must have at randomization a conventional clinic systolic/diastolic BP < 160/100 mmHg.
• Informed consent to participate in the study prior to any study procedures.

Exclusion Criteria

• Known or suspected contraindications, including history of allergy to ASA.
• Uncontrolled essential hypertension of Grade 2-3, i.e., systolic BP ≥ 160 mmHg and/or diastolic BP ≥ 100 mmHg before randomization.
• Evidence of a secondary form of hypertension, to include coarctation of the aorta, hyperaldosteronism, renal artery stenosis, or pheochromocytoma.
• Known Keith-Wagener grade III or IV hypertensive retinopathy.
• History of hypertensive encephalopathy, cerebrovascular event, transient ischemic cerebral attack, or myocardial infarction prior to randomization.
• Type 1 diabetes mellitus.
• History of heart failure.
• Second or third degree heart block without a pacemaker.
• Concomitant unstable angina pectoris.
• Concomitant potentially life threatening arrhythmia or symptomatic arrhythmia.
• Clinically significant valvular heart disease.
• Evidence of hepatic disease as determined by one of the following: ALT or AST values > 2 x UNL known before randomization, a history of hepatic encephalopathy, history of esophageal varices, or history of portocaval shunt.
• Diagnosis of chronic kidney disease prior to randomization.
• History of malignancy including leukemia and lymphoma (but not basal cell skin cancer), or any other severe, life-threatening disease within the past five years.
• Any previous history of a systemic autoimmune disease.
• History of drug or alcohol abuse within the last two years.
• Use of any disallowed concomitant medication.
• Inability to communicate and comply with all study requirements.
• Persons directly involved in the execution of this protocol.

• Minimum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Vigo

OTHER

Sponsor Role: lead

Responsible Party

Ramon C. Hermida

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ramon C Hermida, PhD

Role: STUDY_DIRECTOR

University of Vigo

Locations

CS Friol

Friol, Lugo, Spain

CS Fingoi

Lugo, Lugo, Spain

Complexo Hospitalario Universitario de Ourense

Ourense, Orense, Spain

CS A Estrada

A Estrada, Pontevedra, Spain

CS Baiona

Baiona, Pontevedra, Spain

CS Bueu

Bueu, Pontevedra, Spain

CS A Guarda

La Guardia, Pontevedra, Spain

CS Valmiñor

Nigrán, Pontevedra, Spain

CS Panxón

Nigrán, Pontevedra, Spain

CS Lerez

Pontevedra, Pontevedra, Spain

CS Tomiño

Tomiño, Pontevedra, Spain

Bioengineering & Chronobilogy Labs., University of Vigo

Vigo, Pontevedra, Spain

CS Calle Cuba

Vigo, Pontevedra, Spain

CS A Doblada

Vigo, Pontevedra, Spain

CS Coia

Vigo, Pontevedra, Spain

CS Sardoma

Vigo, Pontevedra, Spain

CS Teis

Vigo, Pontevedra, Spain

CS Vilaboa

Vilaboa, Pontevedra, Spain

CS San Roque

Vilagarcía de Arousa, Pontevedra, Spain

Countries

Spain

Related Links

http://www.hygia.es

Related Info

Other Identifiers

2008-002669-30

Identifier Type: -

Identifier Source: secondary_id

CARING-2008/1

Identifier Type: -

Identifier Source: org_study_id