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Clinical Study on Modified Xiaosheng Liu Decoction Combined with Acupoint Application for Cancer-Related Fatigue with Qi and Yin Deficiency Pattern

Clinical Study on Modified Xiaosheng Liu Decoction Combined with Acupoint Application for Cancer-Related Fatigue with Qi and Yin Deficiency Pattern

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000950
Enrollment
Unknown
Registered
2026-04-13
Start date
2026-04-13
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

cancer-related fatigue,CRF

Interventions

Control group:Based on the patient's current condition, symptomatic treatments such as nutritional support, pain relief, and antiemetic therapy were administered.
Xiaosheng Liu Decoction group:On the basis of the control group, the patients were treated with oral administration of Xiaosheng Liu Decoction. One dose was prescribed per day, decocted in water to 30
Acupoint Application group:On the basis of the control group, acupoint application was administered. Dangshen (Codonopsis Radix), Maidong (Ophiopogon japonicus), and Wuweizi (Schisandra chinensis) wer
Combination group:On the basis of the control group, the patients were treated with combined therapy consisting of oral Xiaosheng Liu Decoction and acupoint application.

Sponsors

People's Hospital of Boluo County, Huizhou, 516100, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age 18–80 years; (2) Meet the diagnostic criteria for malignant tumor and cancer-related fatigue (CRF); (3) Meet the diagnostic criteria for Qi and Yin Deficiency Pattern; (4) Karnofsky Performance Status (KPS) score = 60, with life expectancy > 3 months; (5) Voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Fatigue resulting from excessive exertion that can be relieved by short-term rest; (2) Presence of severe hematologic diseases, or cardiac, hepatic, or renal diseases or complications; (3) Allergy to acupoint application or any component of the oral Chinese herbal formula; (4) Mental or cognitive disorders that may hinder cooperation with treatment; (5) Participation in other drug clinical trials concurrently; (6) Other reasons deemed unsuitable for participation in the clinical trial by the investigators.

Design outcomes

Primary

MeasureTime frame
Fatigue severity;Traditional Chinese Medicine (TCM) syndrome score and its therapeutic efficacy;

Secondary

MeasureTime frame
European Organnization for Research and Treatment of Life Questionnaire-core 30,EORTC OLQ-30;

Countries

China

Contacts

Public ContactFei Li

People's Hospital of Boluo County, Huizhou, 516100, China

leephialf@126.com18933471820

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026