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Study on the Application of Patient-Reported Outcomes (PRO) in Alleviating Postoperative Symptoms in Patients with Early Gastrointestinal Cancer Treated by Endoscopic Submucosal Dissection (ESD)

Study on the Application of Patient-Reported Outcomes (PRO) in Alleviating Postoperative Symptoms in Patients with Early Gastrointestinal Cancer Treated by Endoscopic Submucosal Dissection (ESD)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121859
Enrollment
Unknown
Registered
2026-04-05
Start date
2026-04-06
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Early-stage esophageal, gastric, and colorectal cancers

Interventions

Observation group of patients' self-reported outcomes:None

Sponsors

Bejing Tongren Hospital, Capital Medical Uniersity
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-90 years; 2.Signed informed consent form obtained.

Exclusion criteria

Exclusion criteria: 1.Underwent additional surgical intervention due to ESD failure or off-label indications. 2.Refusal to sign informed consent form.

Design outcomes

Primary

MeasureTime frame
Postoperative Discomfort Symptoms;—

Countries

China

Contacts

Public ContactBin Chuxuan

Bejing Tongren Hospital, Capital Medical Uniersity

cxbin911@126.com+86 10 5853 3225

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026