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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03410654
Other study ID # 2000022307
Secondary ID 000
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date October 24, 2018
Est. completion date December 31, 2024

Study information

Verified date March 2024
Source Yale University
Contact Elizabeth Cohen, PharmD
Phone 203-688-1841
Email elizabeth.cohen@ynhh.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if cognitive function improves in patients converted from tacrolimus immediate release (TAC IR) to Envarsus XR® (tacrolimus extended release) using an objective measure of cognition.


Description:

To assess cognitive function while on TAC IR and then three months after conversion to TAC XR using a traditional cognitive assessment, Montreal Cognitive Assessment (MoCA), and a broader cognitive assessment. This assessment will be used to determine if there is an objective improvement in cognitive function after conversion from TAC IR to TAC XR in kidney transplant recipients.


Recruitment information / eligibility

Status Recruiting
Enrollment 35
Est. completion date December 31, 2024
Est. primary completion date July 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Post-renal transplant on stable TAC IR for at least 6 months who are converting to TAC XR regardless of indication. - Patients receiving their post-transplant care through the Yale-New Haven Transplantation Center (YNHTC) regardless of where they were originally transplanted. Exclusion Criteria: - History of dementia or stroke - Reside in a nursing home - Newly started on an opiate, amphetamine, or benzodiazepine - Non-English speaking (due to lack of NIH toolbox assessments in other languages) - Patients that exhibit signs of acute infection, hemodynamic compromise or other signs of critical illness (e.g. respiratory distress requiring mechanical ventilation) - Recipients of a multiorgan transplant - Pregnant women - Transplant recipients unable to provide informed consent to participate in this research

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tacrolimus, Extended Release, (Envarsus Xr)
After conversion of tacrolimus immediate release to tacrolimus extended release.

Locations

Country Name City State
United States Yale New Haven Transplantation Center New Haven Connecticut

Sponsors (2)

Lead Sponsor Collaborator
Yale University Veloxis Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary cognitive assessment at baseline cognitive assessment at baseline using MoCA test 7.1 baseline
Primary cognitive improvement from baseline cognitive evaluation from baseline average for adults using NIH Toolbox Cognitive Domain 3 months after enrollment
Secondary MoCA cognitive assessment cognitive assessment using MoCA 7.2 3 months after enrollment
Secondary NIH Toolbox cognitive test NIH Toolbox Flanker Inhibitory Control and Attention Test baseline
Secondary NIH Toolbox cognitive test NIH Toolbox Flanker Inhibitory Control and Attention Test 3 months
Secondary NIH Toolbox cognitive test NIH Toolbox Dimensional Change Card Sort Test baseline
Secondary NIH Toolbox cognitive test NIH Toolbox Dimensional Change Card Sort Test 3 months
Secondary NIH Toolbox cognitive test NIH Toolbox Picture Sequence Memory Test Version A baseline
Secondary NIH Toolbox cognitive test NIH Toolbox Picture Sequence Memory Test Version B 3 months
Secondary NIH Toolbox cognitive test NIH Toolbox Pattern Comparison Processing Speed Test baseline
Secondary NIH Toolbox cognitive test NIH Toolbox Pattern Comparison Processing Speed Test 3 months
Secondary NIH Toolbox cognitive test NIH Toolbox List Sorting Working Memory Test baseline
Secondary NIH Toolbox cognitive test NIH Toolbox List Sorting Working Memory Test 3 months
Secondary NIH Toolbox cognitive test NIH Toolbox Reading Recognition Test baseline
Secondary NIH Toolbox cognitive test NIH Toolbox Reading Recognition Test 3 months
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