The Role of Blood Perfusion in Cervical Cancer, Cervical Intraepithelial Neoplasm and Ovarian Cancer Patients
1 other identifier
observational
100
1 country
2
Brief Summary
This study will elucidate the role of 3D transvaginal ultrasound in assessing (1) cervical vascularity and blood flow in patients with cervical cancer and cervical intraepithelial neoplasm, and (2) tumor vascularity and blood flow in patients with ovarian cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2026
Longer than P75 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 13, 2026
CompletedStudy Start
First participant enrolled
January 19, 2026
CompletedFirst Posted
Study publicly available on registry
February 4, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2030
February 4, 2026
January 1, 2026
5 years
January 13, 2026
January 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Vascularization-flow index
1. Compare the vascularization-flow index values between cervical cancer, cervical intraepithelial neoplasia and the control group. 2. To assess whether vascularization-flow index is a predictor of progression-free survival in women with ovarian cancer
3 years
Secondary Outcomes (2)
Vascularization index
3 years
Flow index
3 years
Study Arms (4)
cervical cancer
cervical cancer patients
cervical intraepithelial neoplasm
cervical intraepithelial neoplasm patients
control
Gynecological patients without cervical disease
ovarian cancer
ovarian cancer patients
Interventions
3D doppler ultrasound to measure VI, FI, VFI.
Eligibility Criteria
Women with cervical cancer, cervical intraepithelial neoplasm, ovarian cancer, and the disease-free control
You may qualify if:
- Regarding the topic "Hemoperfusion characteristics of cervical cancer and precancerous lesions, and the correlation between hemoperfusion and prognosis":
- Adult women who have had a normal cervical smear within the past three years and have no other gynecological cancers (control group).
- Adult women with cervical cancer or precancerous lesions.
- Regarding the topic "Correlation between hemoperfusion and prognosis of ovarian cancer":
- Adult women suspected of having ovarian cancer, fallopian tube cancer, or peritoneal cancer before surgery.
You may not qualify if:
- Regarding the topic "Hemoperfusion characteristics of cervical cancer and precancerous lesions of the cervix, and the correlation between hemoperfusion and prognosis":
- \. Patients who cannot cooperate with vaginal 3D ultrasound scans.
- Regarding the topic "Correlation between hemoperfusion and prognosis of ovarian cancer":
- Patients who cannot cooperate with vaginal or abdominal 3D ultrasound scans.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Department of Obstetrics and Gynecology, Far Eastern Memorial Hospital,
New Taipei City, Banqiao, 22050, Taiwan
Far Eastern Memorial Hospital
New Taipei City, 220, Taiwan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 3 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief, Department of Obstetrics & Gynecology
Study Record Dates
First Submitted
January 13, 2026
First Posted
February 4, 2026
Study Start
January 19, 2026
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
December 31, 2030
Last Updated
February 4, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share