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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02177643
Other study ID # 07943212.5.2002.0053
Secondary ID CAAE: 07943212.5
Status Recruiting
Phase Phase 2
First received June 23, 2014
Last updated September 15, 2015
Start date January 2013

Study information

Verified date September 2015
Source University of Campinas, Brazil
Contact Dra. Maria Cândida R. Parisi, PhD
Phone +55 (019) 981962242
Email emaildacandida@uol.com.br
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Considering that, Diacerein is on the market for almost 20 years, being used continuously in elderly patients with osteoarthritis without present significant side effects, and considering the anti-hyperglycemic effect and the improvement in the insulin resistance observed in animal models of type 2 diabetes and in a previously study from Mexico. The aim of our study is to investigate the effect of Diacerein, a medication with anti-osteoarthritic properties and moderately analgesic activity, anti-inflammatory and antipyretic, which demonstrates inhibit properties for the synthesis of pro-inflammatory cytokines such as interleukin 1 (IL-1). Administered for 12 weeks and the effect in the glycemic and metabolic control in patients with diabetes mellitus 2 and secondary failure to metformin treatment.


Description:

This proof of concept study aims to access the metabolic control in patients with type 2 diabetes mellitus and secondary failure to metformin.

The Study is a Phase II, Multicenter, National, Prospective, Randomized, Double blind, Parallel Groups, Placebo Comparative Trial. UNICAMP (Hospital of Unicamp) is the coordinating center and we have the participation of the State University of Feira de Santana and the Center for Diabetes and Hypertension in Fortaleza.

Study Objectives: To investigate the effect of Diacerein administered for 12 weeks; glycemic and metabolic control in patients with diabetes mellitus 2 and secondary failure to metformin treatment. The Total Number of patients will be approximately 60, 30 patients in each group.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Diabetes mellitus (DM) type 2 between 6 months to 10 years of disease

- Body mass index between 25 and 35 kg/m2

- Fasting glucose between 120 and 250 mg/dL

- Glycated Hb A1c greater than 7,5 %

- Taking Metformin (dose above 1700 mg/day) with or without other secretagogue.

Exclusion Criteria:

- Subjects with DM1

- Subjects with DM2 using insulin

- Subjects with DM2 with chronic complications that already have clinical consequences

- Subjects with other types of diabetes

- Creatinine serum greater than 1.4 mg/dl (female) and 1.5 mg/dl (male)

- History of heart disease and/or severe concomitant diseases such as liver, coronary artery, renal

- History of severe psychiatric or neurological disorders

- History of alcohol abuse and/or illegal drugs or psychotropic medicines in the past six months

- Hypersensitivity to any component of the of study drug and placebo formulation.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Intervention

Drug:
Diacerein
Diacerein oral capsules
Placebo
Placebo oral capsules

Locations

Country Name City State
Brazil Universidade Estadual de Campinas Campinas São Paulo
Brazil Universidade Estadual de Feira de Santana Feira de Santana Bahia
Brazil Centro de Estudos em Diabetes e Hipertensão Fortaleza Ceará

Sponsors (3)

Lead Sponsor Collaborator
University of Campinas, Brazil ANS Pharma, Conselho Nacional de Desenvolvimento Científico e Tecnológico

Country where clinical trial is conducted

Brazil, 

References & Publications (4)

Ramos-Zavala MG, González-Ortiz M, Martínez-Abundis E, Robles-Cervantes JA, González-López R, Santiago-Hernández NJ. Effect of diacerein on insulin secretion and metabolic control in drug-naive patients with type 2 diabetes: a randomized clinical trial. Diabetes Care. 2011 Jul;34(7):1591-4. doi: 10.2337/dc11-0357. Epub 2011 May 24. — View Citation

Tobar N, Oliveira AG, Guadagnini D, Bagarolli RA, Rocha GZ, Araujo TG, Prada PO, Saad MJ. Comment on: Ramos-Zavala et al. Effect of diacerein on insulin secretion and metabolic control in drug-naïve patients with type 2 diabetes: a randomized clinical trial. Diabetes Care 2011;34:1591-1594. Diabetes Care. 2012 Feb;35(2):e13; author reply e14. doi: 10.2337/dc11-1856. — View Citation

Tobar N, Oliveira AG, Guadagnini D, Bagarolli RA, Rocha GZ, Araújo TG, Santos-Silva JC, Zollner RL, Boechat LH, Carvalheira JB, Prada PO, Saad MJ. Diacerhein improves glucose tolerance and insulin sensitivity in mice on a high-fat diet. Endocrinology. 2011 Nov;152(11):4080-93. doi: 10.1210/en.2011-0249. Epub 2011 Sep 6. — View Citation

Velloso LA, Folli F, Perego L, Saad MJ. The multi-faceted cross-talk between the insulin and angiotensin II signaling systems. Diabetes Metab Res Rev. 2006 Mar-Apr;22(2):98-107. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Fasting Glucose Concentration Baseline, 12 weeks No
Primary Fasting Insulin Concentration Baseline, 12 weeks No
Primary HbA1c - glycated haemoglobin Baseline, 12 weeks No
Primary Inflammatory Activity Profile TNFa IL6 IL1ß C-Reactive Protein (CRP) Baseline, 12 weeks No
Primary Lipid Panel Baseline, 12 weeks No
Primary Hepatic Function Panel Baseline, 12 weeks No
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