- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07141823
- Original Trial
Oxidative DNA Damage Enhancement by Vitamin C Among Narghile Smokers and Non-smokers (DNA Damage)
August 24, 2025 updated by: Nora Tariq Mohammed
This study aims to evaluate oxidative DNA damage among hookah smokers compared to non-smokers by measuring biomarkers of oxidative stress in blood samples.
The objective is to determine the impact of hookah smoking on DNA integrity and overall oxidative status in adults.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Hookah smoking has become increasingly popular in many regions, yet its potential impact on oxidative stress and DNA integrity is not fully understood.
This study aims to investigate the level of oxidative DNA damage among hookah smokers compared to non-smokers by analyzing biomarkers in blood samples.
A case-control observational design will be used, involving two groups of adult participants: regular hookah smokers and age-matched non-smokers.
Blood samples will be collected from all participants and analyzed for markers of oxidative stress, including 8-hydroxy-2'-deoxyguanosine (8-OHdG) and malondialdehyde (MDA), using validated biochemical methods.
The findings are expected to provide insights into the biological consequences of hookah smoking and support the development of public health interventions.
Study Type
Interventional
Enrollment (Actual)
96
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
semel
-
Dihok, semel, Iraq
- University of Duhok
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Adults aged 18-30 years
Current narghile (hookah) smokers for at least 1 year
Willing to provide informed consent
Exclusion Criteria:
- Healthy participant
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Narghile nonsmokers vitamin C taking
this group of participant take vitamin C for one month, and they are healthy volunteers
|
|
|
Experimental: Narghile smokers
this group take vitamin c supplent for one month period and are healthy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Oxidative DNA damage
Time Frame: Baseline and after 1 month
|
Measurement of plasma MDA concentration using the thiobarbituric acid reactive substances (TBARS) method to assess oxidative stress in participants before and after 1-month Vitamin C supplementation and measuring oxidative stress marker and TAOC
|
Baseline and after 1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 15, 2024
Primary Completion (Actual)
December 10, 2024
Study Completion (Actual)
March 10, 2025
Study Registration Dates
First Submitted
July 16, 2025
First Submitted That Met QC Criteria
August 24, 2025
First Posted (Estimated)
August 26, 2025
Study Record Updates
Last Update Posted (Estimated)
August 26, 2025
Last Update Submitted That Met QC Criteria
August 24, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UoD-ODNS-2025-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
Yes
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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