The Organ Transplant Recipient HPV and Skin Cancer Study
Launched by MERETE HAEDERSDAL · Mar 9, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The Organ Transplant Recipient HPV and Skin Cancer Study is looking into how long-term treatment after receiving an organ transplant affects the risk of skin cancer and HPV-related cancers, such as cervical cancer. People who have had organ transplants need to take medications that weaken their immune system to prevent their body from rejecting the new organ. This makes them more vulnerable to certain types of cancer, and the study aims to gather important information about these risks. Researchers will study 1,800 participants, including 600 male and 600 female organ transplant recipients and 600 healthy controls, to better understand how immunosuppressive therapy impacts their health over time.
To be eligible for the study, organ transplant recipients must be at least 18 years old, have received a solid organ transplant (like a kidney, liver, lung, or heart), and have been on stable medication for at least three months. Participants will have their health monitored through clinical check-ups and data from national health registries. The goal is to improve cancer prevention and provide tailored screening recommendations based on individual risk factors. If you're considering participating, you'll be helping researchers learn how to keep organ transplant recipients safer from skin and HPV-related cancers.
Gender
ALL
Eligibility criteria
- Inclusion Criteria for OTRs:
- • Patients aged ≥18 years
- • Solid organ transplantation recipients, i.e. kidney-, liver-, lung-, and heart transplant recipients
- • Stable immunosuppressive treatment for ≥3 months
- • No signs of acute graft rejection
- • Patients who reside in Denmark
- • Informed written consent obtained
- Exclusion Criteria for OTRs:
- • Patients with concomitant bone marrow transplantation
- • Full hysterectomy
- Inclusion Criteria for Control group:
- • Able patients aged ≥18 years
- • No known immunosuppressive therapy or -condition
- • Patients who reside in Denmark
- • Informed written consent obtained
- Exclusion Criteria for Control group:
- • - Full hysterectomy
About Merete Haedersdal
Merete Haedersdal is a distinguished clinical trial sponsor recognized for its commitment to advancing medical research and innovation. With a focus on dermatology and aesthetic medicine, the organization specializes in the development and evaluation of cutting-edge treatments and technologies. By fostering collaborations with leading researchers and healthcare professionals, Merete Haedersdal aims to enhance patient outcomes and contribute to the evidence-based practice in the healthcare field. Their rigorous approach to clinical trials ensures the highest standards of safety, efficacy, and ethical conduct, reflecting a dedication to improving quality of life through scientific advancement.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Copenhagen Nv, Region Hovedstaden, Denmark
Hellerup, Region Hovedstaden, Denmark
Roskilde, Region Sjælland, Denmark
Roskilde, , Denmark
Patients applied
Trial Officials
Merete Hædersdal, DMSc, MD
Principal Investigator
Bispebjerg Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials