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CaptHPV : Validation of the Method "CaptHPV" for the Diagnosis of Human Papillomavirus Associated Infiltrating Carcinomas

I

Institut de Cancérologie de Lorraine

Status

Completed

Conditions

Penis Cancer
Anal Cancer
Oropharynx Cancer
Vulvar Cancer
Oral Cavity Cancer
Cervical Cancer

Treatments

Other: CaptHPV method

Study type

Interventional

Funder types

Other

Identifiers

NCT02981862
2016-A01085-46

Details and patient eligibility

About

The current project is based on the assumption that a diagnosis of human papillomavirus associated Infiltrating Carcinomas can be made from a blood sample for patient with Cervical Cancer, Vulvar Cancer, Anal Cancer, Oropharynx Cancer, Oral Cavity Cancer or Penis Cancer at any stage of the disease and including surgical treatment for the small tumors.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age >18 years
  • Patient with cervical cancer, vulvar cancer, anal cancer, oropharynx cancer, oral cavity cancer or penis cancer
  • Patient naive of any treatment for this pathology
  • Patient capable and willing to follow all procedures of the study in accordance with the study
  • Ability to provide an informed written consent form
  • Affiliation to a social security system

Exclusion criteria

  • Patients who have already undergone surgical treatment leading to complete removal of the lesions or who have started treatment with radiotherapy and / or chemotherapy
  • Patient whose health status contraindicates a blood sample of 20 ml,
  • Absence of informed written consent form
  • Pregnant or breast feeding females
  • Patients deprived of liberty or under supervision

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

CaptHPV method
Experimental group
Treatment:
Other: CaptHPV method

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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