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Completed

NCT Number: NCT02323997

Human Papillomavirus in Cervical Cancer and Pre-cancer in Switzerland: The CIN3+Plus Study

This study will investigate the types of HPV in samples from women with cervical pre-cancer and cancer and gather information to help investigate the impact of HPV vaccination in Switzerland.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Viollier AG, Allschwil, Basel-Landschaft, Switzerland

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant is willing and able to give informed consent for participation in the study.
  • Participant is literate in German, French, Italian or English.
  • Female, aged 18 years or above.
  • Histologically confirmed CIN3+ lesions, i.e. CIN3, adenocarcinoma in situ and invasive carcinoma of the cervix.
  • Participant resides in the canton Zurich, Geneva, Basel, Baselland, Luzern or Ticino.

Exclusion criteria

  • None

Treatment and study plan

Primary outcomes

  1. Human papillomavirus presence and type

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

University of Bern

Other

Collaborators

  • Federal Office of Public Health, Switzerland

Registry information

Official study title

Human Papillomavirus-Associated Cervical Neoplasia in Switzerland at the Start of a National Vaccination Programme: Crosssectional Study

Acronym: CIN3+plus

Important dates

Study start
2015
Primary completion
2015
Study completion
2016
First posted
Dec 24, 2014
Registry last updated
Jul 16, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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