NCT06114693

Brief Summary

the primary objective of this study is to identify and analyze parametrers affecting the time of recovery of AKI in critical ill patient ,Specifically, the study aims to:

  1. 1.to identify outcomes of critically ill patients who experienced AKI
  2. 2.Examine the relationship between demographic and clinical variables (e.g., age, gender, comorbidities) and outcome of AKI patient
  3. 3.follow Baseline characteristics and laboratory findings of the patients at the time of admission to the intensive care unit and affecting it at recovery time
  4. 4.Explore the association between psychosocial factors (e.g., depression, anxiety, social support) and outcome of AKI patient at icu

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 26, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

November 2, 2023

Completed
1.2 years until next milestone

Study Start

First participant enrolled

January 1, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2025

Completed
Last Updated

January 13, 2025

Status Verified

November 1, 2024

Enrollment Period

4 months

First QC Date

September 26, 2023

Last Update Submit

January 9, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • parameters as renal arterial resistive index and its effect at recovery time of aki patient at icu

    comorbidities(DM,HTN,cardiac disease ) sepsis Renal arterial resistive index

    1year

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

patients who admitted to the ICU for at least 24 hours and experience AKI

You may qualify if:

  • :adult patients (age ≥ 18 years) who admitted to the ICU for at least 24 hours and experience AKI

You may not qualify if:

  • patients (age \<18 years)
  • Patient who refuse enter study Patient

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Acute Kidney Injury

Condition Hierarchy (Ancestors)

Renal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital Diseases

Central Study Contacts

mohamed abdelmongy mohamed, resident

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Director

Study Record Dates

First Submitted

September 26, 2023

First Posted

November 2, 2023

Study Start

January 1, 2025

Primary Completion

May 1, 2025

Study Completion

September 1, 2025

Last Updated

January 13, 2025

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share