FindTrial
Sign In

The Study on Constructing a Symptom Management Cohort for Esophageal Cancer Radiotherapy Patients Based on Patient-Reported Outcomes (PRO)

The Study on Constructing a Symptom Management Cohort for Esophageal Cancer Radiotherapy Patients Based on Patient-Reported Outcomes (PRO)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089580
Enrollment
Unknown
Registered
2024-09-11
Start date
2024-09-21
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

esophageal carcinoma

Interventions

Qualitative Research:None
Reliability and Validity Verification:None
Observation group:None

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Age = 18 years 2.Pathologically or clinically diagnosed with esophageal cancer and undergoing radiotherapy 3.Able to fully understand the content of this study, capable of self-reporting symptoms, willing and able to comply with follow-up requirements, and voluntarily sign the informed consent form to participate in this study

Exclusion criteria

Exclusion criteria: History of cognitive impairment or mental illness

Design outcomes

Primary

MeasureTime frame
RTS_EC;MDASI-ESO;—

Secondary

MeasureTime frame
Success rate of neoadjuvant therapy completion;NRS;—

Countries

China

Contacts

Public ContactQifeng Wang

Sichuan Cancer Hospital

littlecancer@163.com+86 182 2766 7667

Outcome results

None listed

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