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NCT06034717

Primary Patency in Pediatric Patients With Hemodialysis Access

Status unknown Last updated 13 September 2023
What this trial tests

trial in The Aim of This Study is to Follow up Short Term "3-6 Months"& Mid Term" 6-12months "Outcomes of Vascular Access" Native and Synthetic "in ESRD Pediatrics in 60 participants. Status unknown.

Timeline
1 October 2022
Primary endpoint
28 September 2023
28 September 2023

Quick facts

Lead sponsorAlaa Gameil Abd El-salam Hussien
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment60
Start date1 October 2022
Primary completion28 September 2023
Estimated completion28 September 2023
Sites1 location across Egypt

Conditions studied

Sponsor

Alaa Gameil Abd El-salam Hussien

Who can join

Adults 6 to 18, any sex, with The Aim of This Study is to Follow up Short Term "3-6 Months"& Mid Term" 6-12months "Outcomes of Vascular Access" Native and Synthetic "in ESRD Pediatrics. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Vascular access in the pediatric hemodialysis patients is a challenging,but necessary. It requires proper advance planning to assure that the best permanent access is placeds long life span. It is imperative to have a long-term vision to decrease morbidity in this unique patient population.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06034717.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing