ScienHub Research Support

Soc Recerca

Platform for recruiting volunteers interested in participating in clinical trials aimed at improving medical research and global health.

We connect people interested in contributing to scientific advancement with studies evaluating new treatments and therapies. Volunteers can personally benefit and be part of medical progress by participating in trials that address a variety of conditions.

What is a clinical trial?

A clinical trial is a research study where volunteer individuals participate to test potential new treatments with the aim of determining their safety and efficacy.

Clinical Studies

At present, there are no ongoing trials.

Would you like to participate as a volunteer in future clinical trials?

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Who can participate in a clinical study?

Eligibility to participate in a clinical study depends on several factors and may vary according to the design and specific objectives of each study. Inclusion and exclusion criteria are designed to ensure the safety of participants and the validity of the results. Some criteria include: medical diagnosis, age, health status, medical history and previous treatments, among others.

 

Why participate in a clinical trial?

Participation in clinical trials is essential for the progress of medicine by contributing to the development of more effective and safer treatments.

  • It allows testing and validation of the efficiency and safety of new treatments, drugs, vaccines and procedures.
  • Improve existing treatments by comparing new approaches to current standards of care.
  • Offers the opportunity to test innovative therapies that could represent significant advances in the treatment of diseases.
  • Participants may be the first to benefit from new treatments before they are available to the general public.
  • Contributes to global medical knowledge and assist healthcare professionals in making evidence-based decisions.
  • For diseases without a known cure, participation in clinical studies may offer hope and potentially effective treatment options.

The phases of a clinical trial

  • Pre-clinical phase

    In vitro / animals

    It studies the efficacy and safety of a component or a technique.

  • Phase I

    The main objective is to evaluate safety in humans and guide the most appropriate dosage and administration schedule.

  • Phase II

    It measures efficacy and establishes the optimal dose to achieve the desired response.

  • Phase III

    It evaluates effectiveness and side effects compared to a control group.

  • Phase IV

    It assesses unaddressed aspects such as rare side effects or interactions during post-marketing.

Information of interest

  • ScienHub Research Support

    When a person decides to participate in a clinical study, they are guaranteed a series of rights and also assume various responsibilities that are fundamental to the success and integrity of the research.

  • Rights

    • Right to informed consent
    • Preservation of data confidentiality
    • Withdraw consent and withdraw from the study
    • Receive appropriate and specialized medical care
    • Awareness of risks and benefits
    • Be informed about the progress of the study
    • Review by an ethics committee

  • Responsibilities

    • Compliance with study protocols
    • Communication with the research team
    • Attending scheduled visits
    • Reporting side effects or issues
    • Following data management instructions
    • Continuous commitment
    • Providing a complete medical history

  • Informed Consent

    The decision to participate in a clinical study is personal and should be made voluntarily, without external pressures. Whether individuals are in good health or have a medical diagnosis, they should engage in clinical research only if they feel well-informed and comfortable with the entire process.

  • What to know before starting a study?

    We offer you a guidance guide so that you are aware of the important questions before joining a study. We understand that deciding to participate in a study is a significant step, and our goal is to provide you with all the necessary information. Below, you will find some essential questions that will help you make an informed decision:

  • Information of interest

  • ScienHub Research Support

    When a person decides to participate in a clinical study, they are guaranteed a series of rights and also assume various responsibilities that are fundamental to the success and integrity of the research.

  • Rights

    • Right to informed consent
    • Preservation of data confidentiality
    • Withdraw consent and withdraw from the study
    • Receive appropriate and specialized medical care
    • Awareness of risks and benefits
    • Be informed about the progress of the study
    • Review by an ethics committee

  • Responsibilities

    • Compliance with study protocols
    • Communication with the research team
    • Attending scheduled visits
    • Reporting side effects or issues
    • Following data management instructions
    • Continuous commitment
    • Providing a complete medical history

  • Informed Consent

    The decision to participate in a clinical study is personal and should be made voluntarily, without external pressures. Whether individuals are in good health or have a medical diagnosis, they should engage in clinical research only if they feel well-informed and comfortable with the entire process.

  • What to know before starting a study?

    We offer you a guidance guide so that you are aware of the important questions before joining a study. We understand that deciding to participate in a study is a significant step, and our goal is to provide you with all the necessary information. Below, you will find some essential questions that will help you make an informed decision:

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