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Feasibility study to investigate the effect of Acanthopanax senticosus intake on the cancer related fatigue.

Feasibility study to investigate the effect of Acanthopanax senticosus intake on the cancer related fatigue. - Feasibility study to investigate the effect of Acanthopanax senticosus intake on the cancer related fatigue.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000035464
Enrollment
21
Registered
2019-01-07
Start date
2019-01-07
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

Cancer related fatigue (malaise)

Interventions

Oral intake of 5 tablets with Organic Sun Eleuthro three times a day for 14 days. Oral intake of 30 mL with Sun Eleuthro Extract a day for 14 days. Oral intake of 30 mL with Sun Eleuthro Extract twice

Sponsors

Health Sciences University of Hokkaido
Lead Sponsor
Hokubu Rinsho Co,. Ltd
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: # Advanced cancer patient who can take food orally and whose expected survival time is more than one month. # he score of Brief Fatigue Inventory is more than 3 or more. # Age 20 years and older # Ability to provide and written informed consent. # Patients who are receiving palliative chemotherapy are eligible for study if approved by primary oncologist prior to inclusion.

Exclusion criteria

Exclusion criteria: # The patients who have taken Acanthopanax Senticosus and are not off it for more than 3 months. # Allergy to Acanthopanax Senticosus and/or honey. # Uterus and Ovary cancer patient who are histologically confirmed with estrogen receptor positive. # The patient who received Doxifluridine (FURTULON) chemotherapy. # Uncontrolled hypertension (Blood pressure more than 180/90 mmHg) # Currently taking digoxin formulation. # Co-existence of severe complication. # Pregnant or expected to be pregnant, and breast feeding mother. # Co-existence of endometriosis and myoma uteri. # Unable to provide and written informed consent due to mental disorder. # Concomitant use of drugs which is contraindicated towards Acanthopanax Senticosus.

Design outcomes

Primary

MeasureTime frame
The proportion of the patient whose BFI and FACIT-F can be evaluated at day 28.

Secondary

MeasureTime frame
# The changes in BFI score during registration and day 29. # The changes in FACIT-F subscale score during registration and day 29. # The changes in FACIT-F total score during registration and day 28. # Safety (The frequency of total adverse event). # General condition (assessed by ECOG-PS). # The changes in laboratory data.

Countries

Japan

Contacts

Public ContactTada Masahito

Higashi Sapporo Hospital Administrative department

mtada@hsh.or.jp011-812-2311

Outcome results

None listed

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