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Optimization of Serum Phosphorus Level and Weaning From Mechanical Ventilation

NCT05682846 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 124

Last updated 2023-05-19

No results posted yet for this study

Summary

The goal of this clinical trial is to test the impact of serum phosphorus level optimization on weaning from mechanical ventilation in adult ICU patients in Alexandria University Hospitals.

The main questions it aims to answer are:

* Does serum phosphorus level optimization affect the duration of mechanical ventilation?
* Is serum phosphorus level optimization associated with successful weaning from mechanical ventilation?

In critically ill patients, phosphorus supplementation is done using Sodium glycerophosphate pentahydrate solution.

Conditions

  • Mechanical Ventilation

Interventions

DRUG

Sodium glycerophosphate pentahydrate solution

Glycophos is a 20 ml vial of Sodium glycerophosphate pentahydrate containing 1 mmol glycerophosphate and 2 mmol sodium per ml

Sponsors & Collaborators

  • Alexandria University

    lead OTHER

Principal Investigators

  • Magda A El-Massik, PhD · Professor of Pharmaceutics, Alexandria University

  • Haitham M Tammam, PhD · Associate professor of Critical Care Medicine, Alexandria University

  • Noha A Hamdy, PhD · Assistant Professor of Clinical Pharmacy, Alexandria University

  • Marawan M ElBourini, PhD · Lecturer in Critical Care Medicine, Alexandria University

  • Yasmin M Abd Elghany, PharmD · Master's student in Clinical Pharmacy and Pharmacy Practice, Alexandria University.

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-01
Primary Completion
2023-02-28
Completion
2023-02-28

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05682846 on ClinicalTrials.gov