NCT06123260

Brief Summary

To evaluate Renal outcomes among patients, post liver transplantation at Assiut university.

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
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2023

Status
unknown

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

November 2, 2023

Completed
6 days until next milestone

First Posted

Study publicly available on registry

November 8, 2023

Completed
23 days until next milestone

Study Start

First participant enrolled

December 1, 2023

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2025

Completed
Last Updated

November 8, 2023

Status Verified

November 1, 2023

Enrollment Period

1 year

First QC Date

November 2, 2023

Last Update Submit

November 7, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • calculation the incidence of AKI in Liver transplantation patients

    Determination of the most common risk factor for AKI in liver transplantation patients.

    Baseline

Secondary Outcomes (1)

  • mortality rate

    Baseline

Interventions

renal function testsDIAGNOSTIC_TEST

BUN, eGFR , CBC , Electrolytes , Liver function tests

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

retrospective cohort study will be done to patients post liver transplantation at El Raghy university hospital

You may qualify if:

  • Data of all Patients underwent liver transplants with their reports available at El Raghy university hospital

You may not qualify if:

  • Inadequate data
  • Patients on dialysis more than 8 weeks pre liver transplant.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (7)

  • Feffer SE, Parray HR, Westring DW. Seizure after infusion of aminocaproic acid. JAMA. 1978 Nov 24;240(22):2468. No abstract available.

    PMID: 101682BACKGROUND
  • Rautela GS, Snee RD, Miller WK. Response-surface co-optimization of reaction conditions in clinical chemical methods. Clin Chem. 1979 Nov;25(11):1954-64.

    PMID: 498506BACKGROUND
  • Ramakrishnan R, Mittal S, Ambatkar S, Kader MA. Retinal nerve fibre layer thickness measurements in normal Indian population by optical coherence tomography. Indian J Ophthalmol. 2006 Mar;54(1):11-5. doi: 10.4103/0301-4738.21608.

    PMID: 16531664BACKGROUND
  • Braun OH, Kreipe U. [Rare forms of chronic osteomyelitis in children (author's transl)]. Klin Padiatr. 1979 Sep;191(5):511-21. German.

    PMID: 574584BACKGROUND
  • Pannuti F. Surgical adjuvant hormone therapy in breast cancer. Arch Geschwulstforsch. 1978;48(7):680-2. No abstract available.

    PMID: 736749BACKGROUND
  • Pozenel H. [The influence of mexiletin on ventricular arrhythmias during ergometric exercise (author's transl)]. Wien Klin Wochenschr. 1977 Dec 9;89(23):783-8. German.

    PMID: 595602BACKGROUND
  • Blom E. A decapitated sperm defect in two sterile Hereford bulls. Nord Vet Med. 1977 Mar;29(3):119-23.

    PMID: 870880BACKGROUND

MeSH Terms

Interventions

Kidney Function Tests

Intervention Hierarchy (Ancestors)

Diagnostic Techniques, UrologicalDiagnostic Techniques and ProceduresDiagnosis

Study Officials

  • Bahaa Osman Taha, Master

    Bahaa_osman99@aun.edu.eg

    STUDY DIRECTOR

Central Study Contacts

Ebram Magdy Eskander, M.B.B.Ch

CONTACT

Refaat Fathy Abd elaal, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
doctor

Study Record Dates

First Submitted

November 2, 2023

First Posted

November 8, 2023

Study Start

December 1, 2023

Primary Completion

December 1, 2024

Study Completion

January 1, 2025

Last Updated

November 8, 2023

Record last verified: 2023-11