Actively Recruiting
To Evaluate the Efficacy of Oral Molecular Hydrogen Supplement in Patients With Chronic Diseases
Led by HoHo Biotech · Updated on 2024-05-07
60
Participants Needed
2
Research Sites
37 weeks
Total Duration
On this page
Sponsors
H
HoHo Biotech
Lead Sponsor
T
Taoyuan Armed Forces General Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The supplementation of hydrogen molecules as an aid, adjuvant, may speed up recovering the course of the disease. The purpose of this study is to determine the possible efficacy and safety of solid hydrogen supplements for a clinical study in patients with chronic diseases. Patients will receive hydrogen capsules with their conventional treatment for 24 weeks. Investigators will test for any changes in haematologic, urine analysis and health status during and following the exposure period.
CONDITIONS
Official Title
To Evaluate the Efficacy of Oral Molecular Hydrogen Supplement in Patients With Chronic Diseases
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 20 to 80
- Able to compliant with the protocol
- Able to return to the hospital regularly
- Patients with chronic inflammation, including patients with autoimmune diseases, metabolic-related diseases, chronic kidney disease or nephritis, tumor patients, etc.
You will not qualify if you...
- Pregnancy
- Expected pregnancy
- Attending other clinical trials with 6 months
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Tri-Service General Hospital
Taipei, Taiwan
Actively Recruiting
2
Taoyuan Armed Forces General Hospital
Taoyuan, Taiwan
Actively Recruiting
Research Team
K
Kuang-Yih Wang, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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