Inflammatory Cytokines and Oxidative Stress Biomarkers in Diabetic Chronic Kidney Disease Patients (NCT07657286) | Clinical Trial Compass
RecruitingNot Applicable
Inflammatory Cytokines and Oxidative Stress Biomarkers in Diabetic Chronic Kidney Disease Patients
Egypt60 participantsStarted 2026-06-07
Plain-language summary
This research intends to analyze how a 12-week adjustment in lifestyle influences inflammatory cytokines and oxidative stress indicators in overweight individuals diagnosed with type 2 diabetes and moderate CKD
Who can participate
Age range
36 Years – 58 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* sedentary lifestyle for at least three months prior to enrollment
* body mass index (BMI) of 30-35 kg/m².
Exclusion Criteria:
* using tobacco
* heart failure
* coronary arteries
* severe heart valve problems
* pregnant
* liver inflammation
* kidney transplant
* physical injuries restricting them from exercising
* utilization of anti-inflammatory medications
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial is measuring inflammatory markers like IL-6, TNF-α, and CRP, as well as oxidative stress markers like MDA, GSH, GPx, and SOD — what would my own current levels of these markers tell us about how my diabetes and kidney disease are interacting, and is that information something we'd track regardless of this trial?
2Since this study is listed as Phase NA, it sounds more like an observational or measurement study rather than one testing a new treatment — can you help me understand whether joining would involve any new interventions, or would it mainly mean providing blood samples and data?
3How would participating in this trial actually affect my current care plan for my chronic kidney disease and diabetes — would anything change about my medications, monitoring schedule, or doctor visits?
4Given that this trial is actively recruiting, what's the time commitment involved, and are there any risks or burdens I should weigh, such as extra blood draws or clinic visits, that might be difficult given my current health?
5Are there standard-of-care tests or treatments for diabetic chronic kidney disease that we should be prioritizing first, and would taking part in this observational research in any way delay or complicate those options?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.