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Possible Ameliorating Effect of N- Acetylcysteine (NAC) on Type-II Diabetes Induced Nephropathy

Possible Ameliorating Effect of N- Acetylcysteine on Type-II Diabetes Induced Nephropathy

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04531163
Acronym
(NAC)
Enrollment
60
Registered
2020-08-28
Start date
2019-10-01
Completion date
2020-12-01
Last updated
2020-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Kidney Disease, Diabetes Mellitus, Type 2, Diabetic Nephropathies

Keywords

N-Acetyl cysteine, Lipoprotein a, Triglycerides, Total cholesterol, Glycated Haemoglobin, Fasting blood sugar, Serum creatinine, Blood urea nitrogen, Urine analysis, High density lipoprotein, Low density lipoprotein

Brief summary

The study is focused on the possible improving effect of N-acetylcysteine on nephropathy of type-2 diabetic patients. Study design: Prospective clinical based study. The aim of this work is to study the effect of N-acetylcysteine (NAC) on proteinuria and on the serum level of lipoprotein a (LPa) in diabetes induced nephropathy in type-2 diabetic patients.

Detailed description

This study will be carried on 60 participants with Type 2 Diabetes with age over 20 years. Participants will be classified into two groups: 1. Group I (Interventional): treated with (NAC) dose of 1200 mg/day for two months in conjunction with conventional treatment. 2. Group II (Non-interventional): control group receive conventional treatment. All patients will undergo the following: 1. Full medical history will be taken. 2. Laboratory investigations as follows: Blood samples will be collected for analysis after overnight fasting at the beginning and after 2 months of the study for determination of: 1. Total cholesterol (T-chol). 2. Plasma triglycerides (TG). 3. High density lipoprotein cholesterol (HDL-C). 4. Low density lipoprotein cholesterol (LDL-C). 5. Fasting blood sugar. 6. Blood urea nitrogen (BUN). 7. Serum creatinine (SCr). 8. Urine analysis. 9. Glycated hemoglobin (HbA1c). 10. Lipoprotein (a). In addition, blood pressure will be measured for 24 hr.

Interventions

(NAC) is a drug used in the experiment and participant are treated with it by 1200mg/day dose for two months.

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

All participants,investigators, care providers, and outcome assessor have knowledge of the interventions assigned to individual participants.

Intervention model description

Two arms are being used parallel to each other at the same time. Participants are assigned to two groups in parallel for the duration of the study. One arm is interventional assigned to drug administration and the other is a control arm.

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Confirmed diagnosis of Diabetes Mellitus. 2. Age over 20 years. 3. Patients with proteinuria ≥ 30 mg /dl.

Exclusion criteria

1. Patients on lipid lowering medications. 2. Cigarette smokers. 3. Presence of liver and heart diseases.

Design outcomes

Primary

MeasureTime frameDescription
Lipoprotein (a)2 monthsunique lipoprotein that has emerged as an independent risk factor for developing vascular disease.
Triglycerides2 monthsTriglycerides are a type of fat (lipid) found in our blood. It is one of the lipid panel used to determine atherosclerotic risk that contributes to vascular diseases.
Systolic blood pressure2 monthsThe first number of blood pressure reading and it indicates how much pressure our blood is exerting against our artery walls when the heart beats. It is a major risk factor for cardiovascular disease.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026