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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02704494
Other study ID # 93-01-49-9028
Secondary ID
Status Completed
Phase Early Phase 1
First received March 4, 2016
Last updated October 3, 2017
Start date March 2016
Est. completion date February 2017

Study information

Verified date October 2017
Source Shiraz University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the safety and effects of resveratrol in treatment of diabetic nephropathy.


Description:

Diabetes mellitus (DM) is one of the most important public health burdens, and its prevalence has rapidly increased worldwide over the past decades. One of the most important complications of DM is nephropathy.

Resveratrol (3, 5, 4'-trihydroxystilbene) is a natural polyphenolic compound belongs to the large group of polyphenols found in different plant species. The richest natural source of resveratrol is Polygonum cuspidatum — a plant root extract of which have been used in oriental folk medicine. Considerable amounts of resveratrol were also found in skin of red grapes, peanuts, groundnuts, and red vine.

Resveratrol is considered to have beneficial effects on glucose tolerance and insulin sensitivity, the cardiovascular system, as it has been found to improve vasodilatation, ischaemic preconditioning, both of which seem to be the result of the activation of the endothelial NO synthase enzyme, and to inhibit both platelet aggregation and vascular smooth muscle cell proliferation. Resveratrol itself is an efficient antioxidant, as evidenced by both in vitro and in vivo studies, and, it has also been shown to improve diabetes-related impairments in animals.

We hypothesized that resveratrol may have a favorable effects on control of diabetic nephropathy. The aim of this study is to evaluate the safety and effects of resveratrol in treatment of diabetic nephropathy.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Type 2 diabetes mellitus (DM)

- Controlled blood sugar [fasting blood sugar (FBS) <130mg/dl and glycosylated hemoglobin (A1C)<7%

- Urine albumin >20mg/lit in two separate occasions during the last 3 months period

- Serum creatinin < or = 2mg/dl

Exclusion Criteria:

- Pregnancy

- Lactation

- Alcoholism

- Liver failure (acute or chronic)

- Renal failure: serum creatinin >2mg/dl

- Glomerulonephritis

- Uncontrolled hypertension

- Congestive heart failure

- Prostate disease

- Malignancy

- Bilateral renal artery stenosis

- Any systemic disease other than DM

- Any infection or rheumatologic disorder

- Use of warfarin

Study Design


Intervention

Drug:
Resveratrol
Resveratrol 500mg daily
Placebo
Placebo 1 capsule daily
Losartan
Losartan 12.5mg daily

Locations

Country Name City State
Iran, Islamic Republic of Shahid Motahhari Clinic, Shiraz University of Medical Sciences Shiraz Fars

Sponsors (1)

Lead Sponsor Collaborator
Shiraz University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Urine albumin level 3 months
Primary Serum creatinin 3 months
Secondary Fasting blood sugar (FBS) 3 months
Secondary Glycosylated hemoglobin (A1C) 3 months
Secondary Liver aminotransferases (ALT and AST) 3 months
Secondary Serum insulin level 3 months
Secondary Number of patients with adverse events 3 months
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