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Recruiting

NCT Number: NCT01204944

Swiss Transplant Cohort Study

The Swiss Transplant Cohort Study is an observational prospective cohort study enrolling all patients after solid organ and stem cell transplantation since 5/2008 in Switzerland. Predefined variables are collected at defined time points. Individual samples (PBMC, plasma, DNA) will be stored for future projects. Data relevant to transplantation outcome with emphasis on immunological and infectious complications as well as psychosocial variables will be gathered.

Recruiting

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Key information

Age range

0 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Zurich, Switzerland

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All patients after organ and stem cell (planned 2009) transplantation.

Exclusion criteria

  • No informed consent given

Treatment and study plan

Primary outcomes

  1. Outcome after transplantation

    Time frame: open

    Various endpoints

Study contacts

Contact information is provided by the study sponsor or research team.

01 Studienregister MasterAdmins

CONTACT

+41 (0)44 255 11 11

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Collaborators

  • Cantonal Hospital of St. Gallen
  • University of Basel
  • University of Bern
  • University of Geneva, Switzerland
  • University of Lausanne

Registry information

Acronym: STCS

Important dates

Study start
2008
Primary completion
2028
Study completion
2028
First posted
Sep 17, 2010
Registry last updated
Apr 1, 2025

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.