Skip to content

A Randomized Clinical Trial on Innovative Screening Technologies, Strategies, and Collaborative Service Models for Breast Cancer and Cervical Cancer in China

A Randomized Clinical Trial on Innovative Screening Technologies, Strategies, and Collaborative Service Models for Breast Cancer and Cervical Cancer in China - RCT-InnoScreen project

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082904
Enrollment
Unknown
Registered
2024-04-10
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Cervical, Breast cancer

Interventions

AI-aided US group:AI ultrasound assisted the doctor to complete the ultrasound examination
AI-unaided US group:The doctor completed the ultrasound examination without AI.
Regular HPV group:Regular HPV test
POCT group:HPV POCT test
Self sampling group:Women sampled themselves at home

Sponsors

Cancer Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 64 Years

Inclusion criteria

Inclusion criteria: (1) Breast cancer screening innovative technology: women aged 35-64 years; No visible signs of breast cancer; Ability to understand research procedures; Voluntary written informed consent. (2) Cervical cancer screening innovative technology: women aged 35-64 years; Have a sexual life, have an intact uterus, and have no visible signs of typical cervical cancer; Ability to understand research procedures; Voluntary written informed consent. (3) Cervical cancer screening is difficult to reach the population: women aged 35-64 years, sexual life, complete uterus, no visible signs of typical cervical cancer; Have not participated in cervical cancer screening in the past 10 years

Exclusion criteria

Exclusion criteria: (1) Breast cancer screening innovative technology: pregnant, lactating women or planning pregnancy; History of lumpectomy and breast augmentation; Those who have had a percutaneous breast piercing within one year; Previously diagnosed breast cancer patients. (2) Cervical cancer screening innovative technology: pregnancy; History of cervical therapy and pelvic radiation therapy; Patients with previously diagnosed cervical cancer. (3) Cervical cancer screening is difficult to reach the population: pregnancy; History of cervical therapy and pelvic radiation therapy; Patients with previously diagnosed cervical cancer.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;Positive and negative predictive values;

Secondary

MeasureTime frame
Detection rate of breast cancer;Vaginoscopy referral rate;CIN2 detection rate;

Countries

China

Contacts

Public ContactFanghui Zhao

Cancer Hospital, Chinese Academy of Medical Sciences

zhaofangh@cicams.ac.cn+86 158 0156 5892

Outcome results

None listed

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