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Human Phenotype Project Study Protocol

Human Phenotype Project Study Protocol

Recruiting
18 years and older
All
Phase N/A

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Overview

This is a prospective study aimed at recruiting 30,000 individuals, aged 40-70 years old, and following them longitudinally for 25 years with repeated measurements. The basic follow-up frame will include a visit to the Clinical Test Center (CTC) every two years and a phone interview every other year (on uneven years). Sample collection and biobanking will be performed every two years and online questionnaires will be filled out on an annual basis.

The primary goals are to study the variation observed across different individuals in disease susceptibility, clinical phenotypes, and therapeutic responses. The study aims at studying the complex interplay and relative contribution of different omics, physiological characteristics and lifestyle on disease pathogenesis and progression and to evaluate how these effects are mediated.

Eligibility

Inclusion Criteria:

  • Ages 18+, males and females.

Exclusion Criteria:

  • Pregnancy.
  • Mentally disabled or in general legally non-competent.
  • Prisoner or soldier. Soldiers: mandatory service only
  • Active cancer
  • Fertility Treatments (current)
  • Hepatitis ( B, C), chronic or acute
  • HIV
  • Liver cirrhosis
  • Dialysis
  • Unstable medical conditions

Study details
    Adult Disease

NCT05817734

Weizmann Institute of Science

26 January 2024

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FAQs

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What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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