Clinical Trials in China / NCT07656324
Recruiting
Observational
Epidemiology and Prognostic Analysis of Chinese Cancer Patients With Cancer-related Fatigue
NCT07656324 · tracked via the Priya Life Science China tracker
Condition(s) studied
Cancer
Investigational drug(s) / intervention(s)
No Interventions
No Interventions: No Interventions
Study summary
This investigator-initiated study aims to evaluate the incidence and severity of cancer-related fatigue (CRF) in patients with malignant tumors, to analyze the influencing factors of CRF, and to explore its impact on anti-tumor treatment and prognosis.
Eligibility
Inclusion Criteria:
1. Male or female, aged 18 years or older.
2. Able to understand the purpose of this survey study, willing to participate, and able to sign an informed consent form.
3. Malignant tumor confirmed histologically or cytologically.
Exclusion Criteria:
1. Pregnant or breastfeeding women.
2. Patients with acute or chronic infections, or those with other serious medical conditions that, in the investigator's judgment, make them unsuitable for this study.
3. Patients with two or more concurrent malignant tumors (excluding the following: cured basal cell carcinoma of the skin, carcinoma in situ of the cervix, and papillary thyroid carcinoma).
4. Patients with psychiatric illness or mental disorders, poor compliance, or who are unable to cooperate and report treatment responses.
5. Patients with severe organic disease or major organ failure, such as decompensated heart, lung, liver, or kidney failure.
6. Patients with other conditions that, in the investigator's opinion, make them unsuitable for participation in this study.
Primary outcome measure(s)
- The incidence of cancer-related fatigue (CRF) in tumor patients. — Baseline
The incidence of cancer-related fatigue (CRF) in tumor patients.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Fudan University Shanghai Cancer Center | Shanghai | Shanghai Municipality | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07656324 on ClinicalTrials.gov ↗ ← All trials in China