Actively Recruiting

Age: 18Years +
All Genders
NCT06682325

Pharmaco-proteomic Platform to Evaluate Drug Interactions in Liver Transplant Patients

Led by Pontificia Universidad Catolica de Chile · Updated on 2024-11-12

48

Participants Needed

3

Research Sites

100 weeks

Total Duration

On this page

Sponsors

P

Pontificia Universidad Catolica de Chile

Lead Sponsor

U

Universidad de Valparaiso

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to enhance the ability to forecast kidney failure in liver transplant patients in the ICU under multidrug treatment by developing a computer platform that integrates mathematical models of drug interactions, proteomics, and clinical data. The main outcomes it aims to develop are: 1. Design the multidrug web computing platform with available information on drug pair interactions (DDIs). 2. Integrate the proteomic and clinical data of liver transplant patients into the IT platform. 3. Implement the multidrug web platform to predict the clinical evolution of liver transplant patients.

CONDITIONS

Official Title

Pharmaco-proteomic Platform to Evaluate Drug Interactions in Liver Transplant Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Liver transplant patients undergoing surgery at UC Christus Hospital
Not Eligible

You will not qualify if you...

  • Patients on renal replacement therapy
  • Patients for whom no clinical or pharmacological registry is available

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Hospital ClínicoUC-Christus

Santiago, Santiago Metropolitan, Chile, 8330024

Actively Recruiting

2

Pontificia Universidad Católica de Chile

Santiago, Santiago Metropolitan, Chile

Active, Not Recruiting

3

Universidad de Valparaíso

Valparaíso, Valparaiso, Chile

Active, Not Recruiting

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Research Team

N

Nelson Barrera, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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