Collection of cervical cells at colposcopy using a novel technique for analysis of high-risk vs low-risk lesions

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN13994246

Enrollment

387

Registered

2021-09-14

Start date

2017-10-12

Completion date

Unknown

Last updated

2026-04-14

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

Conditions

Cervical cancer Cancer Malignant neoplasm of cervix uteri

Interventions

The patient will be invited to take part in the study. The woman will have been informed that there is an active research programme in the colposcopy clinic. Following consent with the study nurse, th

Eligibility

Sex/Gender

Female

Age

25 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Participant is willing and able to give informed consent for participation in the study 2, Female, aged 25 years or above 3. Diagnosed with abnormal cervical cytology by routine screening

Exclusion criteria

Exclusion criteria: 1. Participant is unable to give consent 2. Pregnant 3. HIV/systemic Immunosuppression

Design outcomes

Primary

Measure	Time frame
Correlation between high-risk and low-risk cervical disease identified using the filter disc and by the standard method	—

Secondary

Measure	Time frame
There are no secondary outcome measures	—

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 17, 2026