Adiponectin and Insulin Resistance in Diabetic Nephropathy

NCT ID: NCT00774904

Last Updated: 2008-10-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-04-30

Study Completion Date

2007-11-30

Brief Summary

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Plasma adiponectin concentration is inversely associated with renal function. There is little literature on adiponectin levels and regulation by antihypertensive medication with an angiotensin II-receptor blocker (ARB), especially in subjects with type 2 diabetes in different stage of chronic kidney disease (CKD).

Detailed Description

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Conditions

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Diabetic Nephropathy

Keywords

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Type 2 Diabetes Diabetic Nephropathy Glucose Metabolism Angiotensin II Type 1 Receptor Blockers

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Losartan

Angiotensin II Type 1 Receptor Blockers

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Type 2 diabetic nephropathy
* CKD at stage 1\~4

Exclusion Criteria

* Type 1 diabetes or nondiabetic renal disease
* An elevated plasma K level.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shanghai Jiao Tong University School of Medicine

OTHER

Sponsor Role collaborator

Xi'an Jiaotong University

OTHER

Sponsor Role lead

Responsible Party

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shanghai No 3 people's hospital

Locations

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Shanghai No.3 people's hospital

Shanghai, , China

Site Status

Countries

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China

References

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Pan Y, Qiao QY, Pan LH, Zhou DC, Hu C, Gu HF, Fu SK, Liu XL, Jin HM. Losartan reduces insulin resistance by inhibiting oxidative stress and enhancing insulin signaling transduction. Exp Clin Endocrinol Diabetes. 2015 Mar;123(3):170-7. doi: 10.1055/s-0034-1395658. Epub 2014 Dec 11.

Reference Type DERIVED
PMID: 25502581 (View on PubMed)

Other Identifiers

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ADPN

Identifier Type: -

Identifier Source: org_study_id