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Effects of Waon therapy in patients with cardiac surgery

Effects of Waon therapy in patients with cardiac surgery - Effects of Waon therapy in patients with cardiac surgery

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007924
Enrollment
120
Registered
2012-05-11
Start date
2012-05-01
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

Patients received cardiac surgery for coronary artely disease or cardiac valvular disease

Interventions

Patients who have standard medical therapy receive Waon therapy once a day for two weeks starting from one week after cardiac surgery Patients who receive standard medical therapy without Waon therapy

Sponsors

The second department of internal medicine, university of Toyama
Lead Sponsor
The first department of surgery, university of Toyama
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who receive cardiac surgery due to coronary artery desease or valvular heart desease

Exclusion criteria

Exclusion criteria: . Hemodynamically unstable . Serious infection . Prior stroke (within 3 months) . Anemia (hemoglobin<8g/dl) . Malignancy . Hematological disorder . Pregnancy . End stage renal desease

Design outcomes

Primary

MeasureTime frame
6-minute walk distance before and after two-week Waon therapy

Secondary

MeasureTime frame
Quality of life score and cardiac function assesed by neurohumoral factors and echo cardiography

Countries

Japan

Contacts

Public ContactTakashi Nozawa

University of Toyama The second department of internal medicine

tnozawa@med.u-toyama.ac.jp076-434-7297

Outcome results

None listed

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