Skip to content

Frailty Among Renal Transplant Recipients and Relation to Chronic Allograft Dysfunction

Study of Frailty Among Renal Transplant Recipients, Its Relation to Chronic Renal Allograft Dysfunction

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07181096
Enrollment
80
Registered
2025-09-18
Start date
2025-07-15
Completion date
2026-01-15
Last updated
2025-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty, Renal Transplant

Keywords

Frailty, renal transplant recipient, chronic allograft dysfunction

Brief summary

The aim of the study is to assess prevalence of frailty among renal transplant recipients in Alexandria University Hospitals and to study the relation between frailty and chronic allograft dysfunction.

Detailed description

With respect to correlates of frailty, although higher comorbidity burden is also a risk factor for frailty among KT candidates, frailty can also occur in the setting of lower comorbidity burdens. Diabetes and serum albumin concentration are also associated with frailty among prevalent dialysis patients. In addition, individuals with CKD and ESKD who are frail are also more likely to have cognitive impairment and sarcopenia, or low muscle mass, than their non-frail counterparts

Interventions

DIAGNOSTIC_TESTassessment of frailty

This study is a prospective cross-sectional study to assess the prevalence of frailty among 80 cases of renal transplanted patients. Specific tests will include: 1. Assessment of frailty by Clinical Frailty Scale. 2. Assessment of nutritional status using Patient Generated Subjective Global Assessment (PG-SGA). 3. Comorbidity assessment using Charlson comorbidity score. 4. Six minutes walk test. 5. Muscle strength assessment using hand grip strength (HGS) dynamometer.

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Renal transplanted patients with GFR more than 30

Exclusion criteria

* Mentally or physically unfit patients. * Amputation of lower limb. * Active neoplasia, chronic liver disease, previous immunological disease. * Psychiatric disorders. * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Assessment of frailty30 daysby Clinical Frailty Scale.

Secondary

MeasureTime frameDescription
Assessment of nutritional status30 daysusing Patient Generated Subjective Global Assessment (PG-SGA)
Comorbidity assessment30 daysusing Charlson comorbidity score
Muscle strength assessment30 daysusing hand grip strength (HGS) dynamometer.

Countries

Egypt

Contacts

Primary ContactMohamed mamdouh Elsayed, MD
dr_mohamedmamdouh87@yahoo.com00201068055103

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026