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The Effects of Atorvastatin on the Nitrogen Oxide-system in Patients With Type 2 Diabetes and Nephropathy (STAD)

Primary Purpose

Nephropathy, Cardiovascular Diseases, Diabetes Mellitus

Status
Completed
Phase
Phase 2
Locations
Denmark
Study Type
Interventional
Intervention
Atorvastatin
Unikalk
Sponsored by
Erling Bjerregaard Pedersen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nephropathy focused on measuring Atorvastatin, L-NMMA, NO, Nephrology, Diabetes Mellitus

Eligibility Criteria

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

Inclusion Criteria:

  • Men and women
  • minimum 40 years
  • Chronic Kidney disease
  • Estimated GFR (eGFR) between 30 and 90 ml/min
  • Diabetes Mellitus type II

Exclusion Criteria:

  • Nephrotic Syndrome
  • Anamnestic or clinical signs of significant heart, lung, lever, kidney and brain disease
  • Neoplastic disease
  • Alcohol abuse,
  • Drug abuse
  • Pregnancy or nursing
  • Blood donation within a month before examination
  • Hgb < 6,0

Sites / Locations

  • Medicinsk Forskning, Regionshospitalet Holstebro

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Atorvastatin

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Fractional excretion of sodium

Secondary Outcome Measures

Systolic blood pressure
Plasma renin concentration
Arterial stiffness
Plasma angiotensin II concentration
Urinary excretion of protein from sodium channels such as the NaCl cotransporter (NCC), the Na-K-Cl cotransporter (NKCC) and the epithelial sodium channel (ENaC)
Augmentations index

Full Information

First Posted
September 19, 2010
Last Updated
August 19, 2015
Sponsor
Erling Bjerregaard Pedersen
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1. Study Identification

Unique Protocol Identification Number
NCT01208701
Brief Title
The Effects of Atorvastatin on the Nitrogen Oxide-system in Patients With Type 2 Diabetes and Nephropathy
Acronym
STAD
Official Title
The Effect of Atorvastatin on the NO-system in Patients With Type 2 Diabetes and Nephropathy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Erling Bjerregaard Pedersen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
It has been documented that statin reduce mortality and morbidity in patients with cardiovascular disease. This effect can partly be related to a reduction in cholesterol levels in blood. Nitric oxide (NO) production is reduced in several chronic diseases such as nephropathy, diabetes and hypertension. The purpose of this study is to investigate the effect of Atorvastatin treatment on the NO-system measuring renal and cardiovascular variables in patients with type 2 diabetes with nephropathy.
Detailed Description
Subjects will be examined on two examination days. 4 days prior to each examination day subjects are treated with either atorvastatin or placebo. During treatment periods subject are given a standardized diet. On the examination days subject are given L-NMMA(L-NG-monomethyl Arginine citrate), a NO inhibitor, 6 mg bolus infusion followed by continuous 4 mg/kg/hr infusion for 1 hour. Renal function, central hemodynamic and vasoactive hormones are evaluated prior, during and after L-NMMA infusion. Renal function is measured by renal clearance of 51Cr-EDTA and urinary sodium, potassium and albumin concentration. Urinary excretion of protein from sodium channels such as the NaCl cotransporter (NCC), the Na-K-Cl cotransporter (NKCC) and the epithelial sodium channel (ENaC) will be measured to evaluate channel activity in the nephron. Central blood pressure, pulse wave analysis, and augmentation index are measured using SphygmoCor® from Atcor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephropathy, Cardiovascular Diseases, Diabetes Mellitus
Keywords
Atorvastatin, L-NMMA, NO, Nephrology, Diabetes Mellitus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Atorvastatin
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Other Intervention Name(s)
Zarator
Intervention Description
Zarator, 80 mg pr day for 5 days
Intervention Type
Drug
Intervention Name(s)
Unikalk
Intervention Description
1 tablet Unikalk pr day for 5 days
Primary Outcome Measure Information:
Title
Fractional excretion of sodium
Time Frame
5 days treatment
Secondary Outcome Measure Information:
Title
Systolic blood pressure
Time Frame
5 days
Title
Plasma renin concentration
Time Frame
5 days
Title
Arterial stiffness
Time Frame
5 days
Title
Plasma angiotensin II concentration
Time Frame
5 days
Title
Urinary excretion of protein from sodium channels such as the NaCl cotransporter (NCC), the Na-K-Cl cotransporter (NKCC) and the epithelial sodium channel (ENaC)
Time Frame
5 days
Title
Augmentations index
Time Frame
5 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women minimum 40 years Chronic Kidney disease Estimated GFR (eGFR) between 30 and 90 ml/min Diabetes Mellitus type II Exclusion Criteria: Nephrotic Syndrome Anamnestic or clinical signs of significant heart, lung, lever, kidney and brain disease Neoplastic disease Alcohol abuse, Drug abuse Pregnancy or nursing Blood donation within a month before examination Hgb < 6,0
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank H Christensen, MD
Organizational Affiliation
Department of Medical Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medicinsk Forskning, Regionshospitalet Holstebro
City
Holstebro
ZIP/Postal Code
7500
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
24256611
Citation
Mose FH, Larsen T, Jensen JM, Hansen AB, Bech JN, Pedersen EB. Effect of atorvastatin on renal NO availability and tubular function in patients with stage II-III chronic kidney disease and type 2 diabetes. Scand J Clin Lab Invest. 2014 Jan;74(1):8-19. doi: 10.3109/00365513.2013.855942. Epub 2013 Nov 21.
Results Reference
derived

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The Effects of Atorvastatin on the Nitrogen Oxide-system in Patients With Type 2 Diabetes and Nephropathy

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