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Urinary Proteomic Assessment of Ovarian Malignancy and Disease Progression

Urinary Proteomic Assessment of Ovarian Malignancy and Disease Progression

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06760923
Enrollment
240
Registered
2025-01-07
Start date
2025-01-01
Completion date
2027-12-31
Last updated
2025-01-07

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

Conditions

Ovarian Cancer (OvCa)

Brief summary

The goal of this observational study is to determine the urinary proteomic characteristics in women with and without ovarian cancer. The main questions it aims to answer are: 1. What is the difference in urinary protein composition between patients with ovarian cancer and those without it? 2. Can these differences in urinary protein composition aid in the diagnosis of ovarian cancer? 3. Are urinary protein markers associated with tumor burden in urine samples from patients with ovarian cancer? 4. Can urinary protein markers be used for disease surveillance in ovarian cancer patients?

Interventions

None listed

Sponsors

Xiangya Hospital of Central South University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female patients in the gynecological ward for surgical treatment. * Initial diagnosis of pelvic mass or malignant ascites may be considered as ovarian cancer; Or the initial diagnosis of ovarian cyst, hydrosalpinx, uterine fibroids or uterine adenomyosis are considered as gynecological non-malignant diseases. * Over 18 years of age. * Voluntary participation and signing of informed consent.

Exclusion criteria

* Study participants with a prior history of malignant tumors. * Study participants with prior chronic kidney disease or renal insufficiency. * Study participants who have received or are receiving treatment for primary disease. * Study participants whose pathological diagnosis was not clear. Any patient should be excluded from the study if: * Study participants withdraw informed consent and request withdrawal. * Study participants were unable to provide a qualified urine sample. * There are situations in which the researcher considers it necessary to withdraw from the study.

Design outcomes

Primary

MeasureTime frameDescription
Pathological diagnosisFrom enrollment to the end of surgery or biopsy at 1 weeksThe histological type of the disease is confirmed by surgery or biopsy

Secondary

MeasureTime frameDescription
ProgressionFrom enrollment to the end of treatment at 6 monthsPatients with ovarian cancer who have recurrent disease after initial treatment with serological or imaging evidence

Countries

China

Contacts

Primary ContactYu Zhang, PhD
xyzhangyu@csu.edu.cn+86 0731-89753999

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026