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OpenTrials
Completed

NCT Number: NCT01580904

Impact of Pharmaceutical Care in Diabetics Patients

The monitoring of diabetics by the pharmacist may contribute to the effectiveness of drug treatment and to improve their quality of life. This study will measure the impact of pharmacotherapeutic follow-up in diabetic patients. This will be a clinical trial, single blind, controlled, randomized, conducted in two units of pharmacies in Brazil. Only in the intervention group will be held the pharmacotherapeutic follow using a methodology called the practice of pharmaceutical care, which identifies and resolves problems related to drugs. The primary outcome is glycated hemoglobin, and secondary outcomes are baseline glucose, total cholesterol and its fractions (for example LDL), all these measures will be made in the intervention group and control group. Patients will be followed for 24 weeks, and the outcomes will be assessed up to 24 weeks. There will be a confidence interval of 95% and a significance of p <0.05, and will use the Student t test, chi-square analysis of variance (ANOVA) and others if necessary. Expects good results and serve as a model for other researchers.

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Key information

Age range

30 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universidade Estadual da Paraíba

João Pessoa, Paraíba, Brazil

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Inclusion criteria:

  • patients aged 30 years,
  • diagnosed with type 2 diabetes,
  • to make use of oral antidiabetic agents with or without insulin

Exclusion criteria

those who had infectious diseases during the research

  • missed three consecutive interviews,
  • suspended the hypoglycemic drug and medical order

Treatment and study plan

Intervention: Pharmaceutical Care

Behavioral

Patients will be followed by the pharmacist by the Pharmaceutical Care Practice

Primary outcomes

  1. Glycated Hemoglobin

    Time frame: Up to 24 weeks

    average glycated hemoglobin over 24 weeks

  2. Fasting Glycemia

    Time frame: Up to 24 weeks

    average fasting glycemia over 24 weeks

Secondary outcomes

  1. Total Cholesterol

    Time frame: Up to 24 weeks

    average total cholesterol over 24 weeks

  2. LDL Cholesterol

    Time frame: Up to 24 weeks

    average LDL cholesterol over 24 weeks

Sponsors and collaborators

Lead sponsor

Universidade Estadual da Paraiba

Other

Collaborators

  • Universidade Federal do Rio Grande do Norte

Registry information

Official study title

Popular Pharmacy of Brazil: Impact of Pharmaceutical Care in Diabetics Patients

Acronym: IPCD

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Apr 19, 2012
Registry last updated
Feb 10, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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