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An observation study of the effect of homologous prescription of medicine and food on chronic fatigue syndrome

An observation study of the effect of homologous prescription of medicine and food on chronic fatigue syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055513
Enrollment
Unknown
Registered
2022-01-11
Start date
2022-01-07
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

chronic fatigue syndrome

Interventions

Sponsors

Hebei College of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male or female participants, aged 18 to 65 years who were diagnosed with CFS according to CDC criteria; According to CDC standards, CFS patients must show the following symptoms: (1) Persistent or recurrent fatigue for 6 months or more, not related to persistent fatigue or any other medical condition related to fatigue; (2) Fatigue and work that significantly interferes with personal activities; (3) Four or more concurrent symptoms (impaired short-term memory or concentration; sore throat; tenderness of cervical or axillary lymph nodes; muscle pain; multiple joint pain without joint swelling or redness; new headache, or severity; unawake sleep; and discomfort lasting more than 24 hours after exercise). 2. Have not received any treatment for CFS in the past 1 month; 3. Voluntarily signed consent forms.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. All kinds of bad habits, such as smoking and drinking within 2 years before the disease; 3. Patients with heart, liver, kidney, brain and other organ dysfunction or mental illness; 4. Patients with chronic fatigue caused by primary or organic diseases; 5. Obese (BMI >= 45); 6. Participate in other clinical trials within 3 months prior to the trial; 7. Allergic constitution or allergic to known ingredients of traditional Chinese medicine.

Design outcomes

Primary

MeasureTime frame
General information questionnaire;The Short-Form (SF-36) Health Survey;Symptoms of fatigue;Fatigue severity scale, FSS;

Countries

China

Contacts

Public ContactLuo Bin

the First Hospital of Hebei Medical University

luobinyisheng@163.com+86 18633889869

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026