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Feasibility of using the Pap-smear as a screening device for the detection of endometrial and ovarian cancer

Feasibility of using the Pap-smear as a screening device for the detection of endometrial and ovarian cancer - Detecting endometrial and ovarian cancer with the Pap-smear

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON39020
Enrollment
150
Registered
2013-11-29
Start date
2014-03-11
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Cervical smear (Pap-smear) uterine cancer (endometrial cancer)

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Endometrial cancer: patient suspected of having endometrial cancer i.e. postmenopausal bleeding Ovarian cancer: patient highly (99% certainty) suspected of having ovarian cancer. This will be based on RMI>200, CA125/CEA ratio, ascites, peritoneal depositions, omental cake or even laparoscopic evaluation.

Exclusion criteria

Exclusion criteria: Previous pelvic radiotherapy

Design outcomes

Primary

MeasureTime frame
The main study parameter is the correlation between mutations found in the Pap-smear and the pipelle endometrial sampling and the primary tumor.

Secondary

MeasureTime frame
The main study parameter is the correlation between mutations found in the vaginal swab and the pipelle endometrial sampling and the primary tumor. To assess the correlation between the results of the mutation analysis and tumour characteristics (histology, stage).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)