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Efficacy of Telmisartan and the Combination of Telmisartan and Ramipril in type1 Diabetes Patients With Nephropathy (START1DM)

Primary Purpose

Diabetic Nephropathy

Status
Completed
Phase
Phase 3
Locations
India
Study Type
Interventional
Intervention
Telmisartan, Ramipril
Sponsored by
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Nephropathy focused on measuring type1 DM, microalbuminuria, nephropathy, albumin excretion rate, dual blockade, ACEI, ARB

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diabetes mellitus by ADA criteria
  • Clinical history of DKA
  • HbA1C < 7.5,urine AER >/= 20 mcg/min on two overnight urine samples

Exclusion Criteria:

  • Pregnancy
  • Unwillingness to use contraception during time of study
  • Creatinine >3 mg/dl
  • Suspected/proven non diabetic nephropathy
  • Active urinary sediment

Sites / Locations

  • Post Graduate Institute of Medical Education and Research

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A

Arm Description

single experimental arm cross over of patients, addition of Ramipril onto Telmisartan.

Outcomes

Primary Outcome Measures

Reduction in albumin excretion rate

Secondary Outcome Measures

24 hr ambulatory BP reduction,nocturnal BP reduction, proportion of dippers

Full Information

First Posted
August 18, 2008
Last Updated
August 19, 2008
Sponsor
Postgraduate Institute of Medical Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT00738660
Brief Title
Efficacy of Telmisartan and the Combination of Telmisartan and Ramipril in type1 Diabetes Patients With Nephropathy
Acronym
START1DM
Official Title
Efficacy of Telmisartan and the Combination of Telmisartan and Ramipril in type1 Diabetes Patients With Nephropathy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
May 2008 (Actual)
Study Completion Date
May 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Postgraduate Institute of Medical Education and Research

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypothesis: The angiotensin receptor blocker telmisartan is effective at reduction of albumin excretion rate(AER) in patients with type1 diabetes and micro or macroalbuminuria. Dual blockade with the addition of ramipril an angiotensin receptor blocker gives added efficacy for reduction of AER. ARB telmisartan gives a 24 hr BP lowering effect. Summary: This is an open label cross over study involving 30 patients who were initially treated with Telmisartan 80 mg for eight weeks followed by addition of Ramipril 10 mg for a further eight weeks. Albuminuria reduction and BP reduction with both clinic and ambulatory BP records were studied at the end of each phase.
Detailed Description
To evaluate the antialbuminuric efficacy of an angiotensin receptor blocker (ARB) telmisartan and the combination of telmisartan and ramipril in patients with type1 DM and either micro or macroalbuminuria.To evaluate the same drugs for their antihypertensive efficacy and their influence on dipping patterns using ambulatory BP monitoring. Methods: Open label cross over study involving 30 patients who were initially treated with telmisartan 80 mg for eight weeks followed by addition of ramipril 10 mg for a further eight weeks. Albuminuria reduction and BP reduction with both clinic and ambulatory BP records were studied at the end of each phase Overnight urine samples of nine hours duration were collected . The volume of urine was verified by measurement in a jar with accuracy of 50ml by the study investigator on every occasion. . Albuminuria was estimated by immuno-turbidimetry Hemocue albumin system Angelholm AD, Sweden (inter assay CV 4.3% ). The albumin excretion rate(AER) at baseline evaluation was determined as the mean AER of the positive urine samples. During subsequent evaluations at the end of 8weeks and at the end of 16 weeks the mean albumin excretion rate from two successive overnight urine samples was taken as the mean .Ambulatory BP (ABP) measurement :ABP was measured using Spacelabs device 90207 Spacelabs inc. use of which is described before(14) .A uniform protocol of inflation once in every 30 min was used. Cuff was applied to the nondominant arm. Recordings were started in all patients between seven and ten AM.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Nephropathy
Keywords
type1 DM, microalbuminuria, nephropathy, albumin excretion rate, dual blockade, ACEI, ARB

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
single experimental arm cross over of patients, addition of Ramipril onto Telmisartan.
Intervention Type
Drug
Intervention Name(s)
Telmisartan, Ramipril
Other Intervention Name(s)
cardace, cardiopri, tazloc
Intervention Description
80 mg of telmisartan administered for 8weeks,followed by addition of ramipril 10 mg for further 8weeks
Primary Outcome Measure Information:
Title
Reduction in albumin excretion rate
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
24 hr ambulatory BP reduction,nocturnal BP reduction, proportion of dippers
Time Frame
8weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diabetes mellitus by ADA criteria Clinical history of DKA HbA1C < 7.5,urine AER >/= 20 mcg/min on two overnight urine samples Exclusion Criteria: Pregnancy Unwillingness to use contraception during time of study Creatinine >3 mg/dl Suspected/proven non diabetic nephropathy Active urinary sediment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
sanjay k bhadada, DM
Organizational Affiliation
Post Graduate Institute of Medical Education and Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Post Graduate Institute of Medical Education and Research
City
Chandigarh
ZIP/Postal Code
1600012
Country
India

12. IPD Sharing Statement

Learn more about this trial

Efficacy of Telmisartan and the Combination of Telmisartan and Ramipril in type1 Diabetes Patients With Nephropathy

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