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Prospective, randomized, open-label,clinical trial comparing the effects of hydrogen tablet and placebo on blood and urine makers for cardiovascular diseases

Prospective, randomized, open-label,clinical trial comparing the effects of hydrogen tablet and placebo on blood and urine makers for cardiovascular diseases - Effects of hydrogen tablet on blood and urine makers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032701
Enrollment
30
Registered
2019-05-24
Start date
2018-05-24
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

cardiovascular disease, diabetes and dyslipidemia

Interventions

hydrogen tablet 2tab/day for 4 weeks &gt
placebo 2tab/day for 4 weeks placebo 2tab/day for 4 weeks &gt
hydrogen tablet 2tab/day for 4 weeks

Sponsors

Tokorozawa Heart Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with cardiovascular diseases, diabetes and dyslipidemia 2) Out patients

Exclusion criteria

Exclusion criteria: 1) Poor-controlled hypertension (DBP>110) 2) Poor-controlled diabetes (HbA1c>8.0 %) 3) Secondary hypertension 4) History of stroke, acute coronary syndrome or any cardiovascular diseases needed for inpatient-treatments within 6 months 5) Either level of aspartate aminotransaminase or alanine aminotransferase exceeds three-fold of the normal limits. 6) End stage renal disease 7) Symptomatic (NYHA III or IV) congestive heart failure 8) Malignancies or other diseases with poor prognosis 9) Subjects whose doctor in charge do not agree to join the trial

Design outcomes

Primary

MeasureTime frame
Markers indicating oxidative stress (Oxidized albumin, isoprostane, 8-OHdG, MDA-LDL, FABP) 4 weeks after administration

Secondary

MeasureTime frame
Blood lipids, glucose, HbA1c Markers indicating obesity (e.g. adiponectin), inflammation (high sensitive CRP), and early-staged kidney diseases (microalbuminuria) 4 weeks after administration

Countries

Japan

Contacts

Public ContactMakoto Ayaori

Tokorozawa Heart Center Shintokoekimae Clinic

ayaori@ba2.so-net.ne.jp04-2929-1801

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026