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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04766450
Other study ID # NAC in DPN
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date December 1, 2021
Est. completion date December 1, 2022

Study information

Verified date August 2022
Source Ain Shams University
Contact Sherien Emara, TA
Phone 01154089169
Email sherienemara@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the current study is to evaluate the efficacy and safety of high dose oral NAC (2400 mg/day divided into two doses) as an adjunct therapy on oxidative stress, inflammatory markers and clinical outcome in patients with type 2 diabetes suffering from diabetic peripheral neuropathy.


Description:

Patient written informed consent will be taken prior to study conductance - Lab assessment will be done at baseline and at the end of the study by withdrawing 7 ml of whole blood for assessment of following parameters: HbA1c, Liver & renal functions - Inflammatory markers including: Human Nuclear factor erythroid 2-related factor (NRF2) & Tumor necrosis factor alpha (TNF-α) using ELISA Kit - Oxidative stress markers: Glutathione Peroxidase using ELISA Kit Inflammatory and oxidative stress marker samples will be stored at -80 for further evaluation using ELISA kit at the end of the study


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 1, 2022
Est. primary completion date November 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: 1. Males or females aged 18-50 years diagnosed with Type 2 Diabetes taking oral hypoglycemic with controlled at HbA1c (6%-7%.) 2. Patients diagnosed with Diabetic Neuropathy (by pinprick, temperature probe, ankle reflex, and vibration perception (128-Hz tuning fork) or pressure sensation (10 g monofilament test). Exclusion Criteria: 1. Patients with acute and chronic inflammatory conditions, consuming any antioxidant supplements or anti-inflammatory medicines. 2. Pregnancy or lactation or expecting to get pregnant during the study. 3. Medical, psychological, or pharmacological factors interfering with the collection or interpretation of study data. 4. Cancer patients. 5. Anyone having hypersensitivity to N-acetylcysteine. 6. Anyone already taking N-acetylcysteine.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Acetyl cysteine
NAC exhibits potent anti-oxidant activity in the cell through augmentation of intracellular GSH, which is a major component of the pathways by which cells are protected from OTS, and its direct scavenging activity of free radicals by providing sulfhydryl groups. Additionally, NAC treatment exhibits anti-in?ammatory effects via inhibition of NF-?B activation and reducing subsequent cytokine production . Mitochondria-protective mechanisms of NAC may also be related to its anti-oxidant and anti-in?ammatory properties

Locations

Country Name City State
Egypt Demerdash Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other Michigan neuropathy screening instrument. Questionnaire of 15 yes or no questions. score of 13 or more means more neuropathic symptoms At baseline and after 3 months
Other Toronto clinical scoring system Questionnaire. as score increase means symptoms increase At baseline and after 3 months
Primary Concentration of Human Nuclear factor erythroid 2-related factor (NRF2) Inflammatory marker change from baseline Human Nuclear factor erythroid 2-related factor at 3 months
Primary Concentration of Tumor necrosis factor alpha Inflammatory marker Change from baseline tumor necrosis factor alpha at 3 months
Primary Concentration of Glutathione peroxidase Oxidative stress markers Change from baseline glutathione peroxidase at 3 months
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