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The impact of intraoperative detection of additional lesions with 68Ga-EB-FAPI radionuclide probe on the prognosis of ovarian cancer

The impact of intraoperative detection of additional lesions with 68Ga-EB-FAPI radionuclide probe on the prognosis of ovarian cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110440
Enrollment
Unknown
Registered
2025-10-14
Start date
2025-10-30
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

ovarian cancer

Interventions

Probe development group:None
Non developing group:None

Sponsors

Beijing Obstetrics and Gynecology Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with ovarian epithelial malignancies, who have extensive implantation and metastasis on enhanced CT/MRI of the pelvis and abdomen, and are diagnosed with FIGO stage II-IV ovarian cancer; 2. Patients who underwent 68Ga-EB-FAPI probe PET/CT examination within 10 days and whose radionuclide imaging showed positive results; 3. Patients without surgical contraindications and expected to undergo R0 resection in cytoreductive surgery; 4. Patients with complete medical records, aged between 18 and 70 years; 5. Patients who can follow the research protocol and undergo regular follow-up; 6. Patients have given consent and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe abnormalities in liver and kidney functions; 2. Those who cannot lie flat for half an hour; 3. Those who cannot tolerate all clinical examinations; 4. Those with tumor cell ablation surgery who cannot undergo R0 resection during the operation; 5. Those with contraindications for surgery and who cannot tolerate it; 6. Those with other malignant tumors; 7. Other situations judged by the researchers as not suitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Two-year progression-free survival rate;

Countries

China

Contacts

Public ContactJinwei Miao; Xinyi Zhang

Beijing Obstetrics and Gynecology Hospital, Capital Medical University

jinweimiao@ccmu.edu.cn+86 188 6366 3255

Outcome results

None listed

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