Participation in Clinical Trials
At CIPREC, we evaluate new therapeutic options, working with specialized teams, ethical processes, and a constant commitment to the well-being of participants.
If you would like to know whether there is an ongoing study in your therapeutic area of interest, please complete your details:
Frequently Asked Questions
The most common questions about clinical research.
Do you have other questions? Contact us.
Participation in a research study is voluntary and does not replace regular medical care.
What is a clinical study?
- It is a medical research study that evaluates a new treatment in people who voluntarily choose to participate.
- It assesses the safety and efficacy of new medications, devices, or treatments.
- These studies are conducted before the treatments become widely available
What is informed consent?
- It is the process by which a person freely and voluntarily confirms their decision to participate in a research study after being informed about all relevant aspects of the study.
- Informed consent is documented through the signing of a specific form.
Who can participate?
- Each study has defined eligibility criteria (such as age, diagnosis, and health status).
- The study team reviews whether the individual meets these requirements.
Is there any cost to participate?
No
What rights do I have as a participant?
- Receive clear information before deciding
- Ask all necessary questions
- Withdraw at any time, without providing an explanation
- Acceder a atención médica durante todo el estudio.
Is it safe to participate?
- Clinical studies comply with international and national regulations.
- Before starting, they are approved by ethics committees and regulatory authorities.
- The medical team closely monitors each participant’s health.
What is the difference between a clinical study and standard treatment?
- In a clinical study: care follows an approved protocol with defined monitoring.
- In standard treatment: decisions are made by the treating physician.
- En ambos casos, la prioridad es la salud del paciente.
Can I withdraw after I have started?
- Yes. Participation is voluntary.
- You may withdraw at any time.
- This will not affect your usual medical care.
What happens to my personal information?
- Your information is handled confidentially.
- Local and international data protection regulations are followed.
- Information shared with the sponsor does not include names or data that could identify the participant.
What kind of follow-up is done during the study?
- Regular medical visits
- Laboratory tests, imaging studies, or other assessments (as defined by the protocol)
- All aimed at evaluating safety and effectiveness.
What happens after the study ends?
- The study team informs the participant about the next steps for their medical care.
- Results are analyzed collectively and contribute to the development of new treatments.