A double-blind, placebo controlled, randomized trial to evaluate the efficacy of SE in post-stroke rehabilitation patients.

A double-blind, placebo controlled, randomized trial to evaluate the efficacy of SE in post-stroke rehabilitation patients. - A double-blind, placebo controlled, randomized trial to evaluate the efficacy of SE in post-stroke rehabilitation patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000012902

Enrollment

Registered

2014-01-27

Start date

2013-11-01

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

Stroke

Interventions

SE(Extract of Citrus species) Placebo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Aged 50 or older 2. Primary disease is first ever stroke 3. Within two weeks after admission 4. SIAS Knee-Extension Test score is within 3 5. Patients who can ride normal wheelchair

Exclusion criteria

Exclusion criteria: 1. Impossible to get informed concent by cognitive deficit 2. Impossible to be treated with exercise therapy due to complication or previous disease 3. Impossible to swallow experimental food 4. Patients who receive parenteral or enteral Nutrition 5. peel of citrus species supplementation 6. Patients who are judged inappropriate for the study by the physician

Design outcomes

Primary

Measure	Time frame
Skeletal muscle mass (BIA, thigh muscle area by Computed tomography)	—

Countries

Japan

Contacts

Public ContactKaoru Honaga

Tokyo Bay Rehabilitation Hospital Rehabilitation Department

rh_fortune@hotmail.com047-453-9000

Outcome results

None listed

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