Acetylsalicylic Acid and Type 2 Diabetes Mellitus

NCT ID: NCT03341117

Last Updated: 2017-11-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

21 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-12-02

Study Completion Date

2016-12-02

Brief Summary

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OBJETIVE To assess the effect of acetylsalicylic acid on antioxidant enzymatic system in patients with type 2 diabetes

Detailed Description

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A randomized, double blind placebo controlled clinical trial was carried out in 21 adult patients with type 2 diabetes. Acetylsalicylic acid 300mg/d was administered orally for 3 months to study group (n=11) and placebo to the control group (n=10).

Conditions

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Diabetes Mellitus, Type 2 Antioxidant Enzyme System

Keywords

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acetylsalicylic acid antioxidant enzyme system stress oxidative type 2 diabetes mellitus.

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

A randomized double blind, placebo controlled clinical trial was carried out in 21 drug naïve adults (35-50 year of age) with DM2 with \<5 years since diagnosis. They were overweight or obese (BMI 25.0 - 35.0 kg/m2), had glycosylated hemoglobin A1C (HbA1c) level between 6.5 - 9%. This protocol study was reviewed and approved by the hospital based ethics committee, and written informed consent was obtained from all volunteers. Subject was selected from the same residential area and socioeconomic status. No participants were excessively sedentary or participated in heavy physical activity. All individuals were nonsmokers. Their body weight was stable for al last 3 months before the study.
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators
A randomized double blind, placebo controlled clinical trial was carried out in 21 drug naïve adults,regimen was prescribed to the subjects.

The allocation was 1:1 concealed and done by simple randomization using a table of random numbers. After randomization, 11 patients received of ASA 300 mg once daily and 10 patients received placebo (calcined magnesia) in the same pharmacological presentation for 90 days, the dose was based in the non-affectation of renal uric acid resorption.

Study Groups

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Acetylsalicylic acid

The patients were randomly assigned to received Acetylsalicylic acid 300 mg once daily for 90 days

Group Type ACTIVE_COMPARATOR

Acetylsalicylic acid

Intervention Type DRUG

Acetylsalicylic acid 300 mg per capsule

calcined magnesia

The patients were randomly assigned to received placebo (calcinaned magnesia),

1 capsule 300 mg before each meal for a period of 90 days.

Group Type PLACEBO_COMPARATOR

Calcined magnesia

Intervention Type DRUG

Calcined magnesia 300 mg per capsule

Interventions

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Acetylsalicylic acid

Acetylsalicylic acid 300 mg per capsule

Intervention Type DRUG

Calcined magnesia

Calcined magnesia 300 mg per capsule

Intervention Type DRUG

Other Intervention Names

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Aspirin Placebo

Eligibility Criteria

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Inclusion Criteria

* Type 2 Diabetes
* BMI 25.0 - 35.0 kg/m2
* HbA1c between 6.5 - 9%.
* Written informed consent
* Same residential area and socioeconomic status.

Exclusion Criteria

* Sedentary or heavy physical activity.
* Nonsmokers.
* Body weight was stable for al last 3 months before the study.
* Personal history of hepatic, renal, gastric or coronary artery disease.
* Hypersensibility to acetylsalicylic acid.
Minimum Eligible Age

35 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Centro Universitario de Ciencias de la Salud, Mexico

OTHER

Sponsor Role lead

Responsible Party

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Sara Pascoe Gonzalez

PhD Clinical Research

Responsibility Role PRINCIPAL_INVESTIGATOR

References

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Other Identifiers

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2345

Identifier Type: -

Identifier Source: org_study_id