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Evaluation of postoperative symptoms and timing prediction of chemotherapy for ovarian cancer based on patient-reported outcome

Evaluation of postoperative symptoms and timing prediction of chemotherapy for ovarian cancer based on patient-reported outcome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094015
Enrollment
Unknown
Registered
2024-12-16
Start date
2024-12-16
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Ovarian cancer

Interventions

Experimental group :Use the symptom management platform and deal with the early warning symptoms
Control group:The symptom management platform was not used

Sponsors

The Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
14 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.The patient has good medical competence and gives informed consent to participate in this clinical study; 2.No surgical dication for ovarian cancer;prepare to receive comprehensive staging surgery of ovarian cancer or tumor reduction surgery; 3.Prepare to receive first-line chemotherapy after the surgery; 4.Have certain reading and writing skills, have the ability to use a smartphone.

Exclusion criteria

Exclusion criteria: 1.Patients with severe primary diseases such as heart, liver and kidney; 2.Severe mental illness or mental illness; no recovery from acute upper respiratory tract infection or asthma onset and persistence; 3.Malignant tumors originating at other sites; 4.Four or more symptom cases had missing data.

Design outcomes

Primary

MeasureTime frame
Interval between postoperative to chemotherapy;Clinical symptoms of patients after surgery to before chemotherapy;

Secondary

MeasureTime frame
Biochemical indicator;

Countries

China

Contacts

Public ContactYuhua Zeng

The Affiliated Hospital of North Sichuan Medical College

2742796290@qq.com+86 817 259 8273

Outcome results

None listed

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