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NCT03776357

A Rehabilitation Tool to Determine Patient's Stay in Hospital After Joint Replacement

Terminated NA Results posted Last updated 30 June 2022
What this trial tests

NA trial testing VERA clinic in Total Joint Replacement Surgery in 9 participants. Terminated before completion.

Timeline
26 August 2019
Primary endpoint
10 March 2020
10 March 2020

Quick facts

Lead sponsorDerek Amanatullah
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposehealth services research
Enrollment9
Start date26 August 2019
Primary completion10 March 2020
Estimated completion10 March 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Derek Amanatullah

Who can join

Adults 18 to 99, any sex, with Total Joint Replacement Surgery. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Length of Stay in Hospital Through Discharge Primary · Up to 2 days
GroupValue95% CI
Experimental22 – 2
Number of Participants Requiring Gait Aid Use Secondary · 3 months post operative visit

The gait aide use ranges in the order of decreasing performance as Nothing \> Cane \> crutch \> walker.

None ( no gait aide)
GroupValue95% CI
Experimental9
Cane
GroupValue95% CI
Experimental0
Crutch
GroupValue95% CI
Experimental0
Walker
GroupValue95% CI
Experimental0
Knee Society Score (KSS) Secondary · 3 months post operative visit

To assess the effectiveness of the device by calculating knee society score (KSS) after surgery. The scale ranges from 0-100 with grading as Score 80-100 - Excellent Score 70-79 - Good Score 60-69 - Fair Score below 60 - Poor

Excellent (80-100)
GroupValue95% CI
Experimental6
Good (70-79)
GroupValue95% CI
Experimental0
Fair (60-69)
GroupValue95% CI
Experimental2
Poor ( below 60)
GroupValue95% CI
Experimental1
Knee Range of Motion Secondary · 3 months post operative visit

To assess the effectiveness of the device by calculating range of motion (maximum degrees)

extension
GroupValue95% CI
Experimental1.1± 2.2
flexion
GroupValue95% CI
Experimental107.8± 17.5

Sponsor's own description

This is the research study of a rehabilitation tool that informs, guides and empowers clinicians to care for their patients. We hope to learn ways to improve patient outcomes, reduce costs and increase value to the healthcare system

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Derek Amanatullah trials

Trials by the same sponsor.

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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/NCT03776357.

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