A Study Of Patient Acceptance Evaluation For The Autonomous Robotic Phlebotomy Device

Overview

About this study

The purpose of the study is to gather exploratory data about patient perception and experiences with a non-functional, non-invasive only version of the Aletta ARPD. A positive perception is of major importance for adoption of the device amongst patients.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Age 22 years and older

 

Exclusion Criteria:

  • Any subjects not meeting the inclusion criteria.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 12/31/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Brooke Katzman

Closed for enrollment

Contact information:

DLMP Research and Innovation Office

(507) 284-9080

DLMPRIO@mayo.edu

More information

Publications

Publications are currently not available