Long-term follow-up on cancer treatment effects and patient quality of life

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to establish a registry that collects data on the safety and effectiveness of innovative anticancer drugs in real-life settings while also measuring the quality of life of patients undergoing these treatments. The Rafael Institute focuses on a patient-centered approach, emphasizing the importance of personalized care and continuous support from a multidisciplinary team. By documenting the relationship between treatment side effects and quality of life, the study seeks to enhance the overall management of cancer patients and address their needs more effectively.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age equal to or greater than 18 years (adult)
* Patients treated with an anticancer drug included in the list of innovative/expensive therapies (protocol appendix)
* Patients benefiting from non-pharmacological treatment at the Rafael Institute
* Who understands the French language

Exclusion Criteria:

* \< 18 years old
* Patient deprived of liberty, under guardianship or unable to give consent

Where it's running

• Institute Rafaël
  Levallois-Perret, Institut Rafael, France Recruiting

Study contacts

• Study coordinator: Alain TOLEDANO, MD
• Email: alain.toledano@horg.fr
• Phone: + 33 (0)1 84 00 70 07

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.