Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India

NCT01995539 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 181

Last updated 2018-12-04

Study results available
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Summary

The purpose of the India iPro2 study is to demonstrate that iPro2 Continuous Glucose Monitoring System (CGMS) evaluation enables Health Care Professional (HCP)s treating patients in India with type 2 diabetes to get a better understanding of their patient's metabolic fluctuations, and support appropriate therapeutic intervention.

Conditions

  • Diabetes Mellitus, Type 2

Interventions

BEHAVIORAL

therapy regimen

Subjects will be recommend changes in therapy regimens.

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY
  • Medtronic Diabetes

    lead INDUSTRY

Principal Investigators

  • Jothydev Kesavadev, MD · Jothydev's Diabetes and Research Centre

  • Mohan V, MD · Madras Diabetes Research Foundation

  • Vijay Viswanathan, MD · M.V Hospital for Diabetes Research centre

  • Ambrish Mithal, MD · Medanta Institute of Clinical Research

  • Manoj Chawla, MD · Lina Diabetes Care Mumbai Diabetes Research Centre

  • Rajiv Kovil, MD · Dr.Kovil's Diabetes Care centre

  • Banshi Saboo, MD · DIA Care

  • Sunil Jain, MD · TOTALL Diabetes Hormone Institute

  • Abhay Mutha, MD · Diabetes Care & Research Center

  • Shehla Shaikh, MD · K.G.N DIABETES AND ENDOCRINE CENTRE

  • Dharmen Punatar, MD · Diab Care Centre

  • Scott Lee, MD · Medtronic Diabetes

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2014-01-31
Completion
2014-04-30

Countries

  • India

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01995539 on ClinicalTrials.gov