Hyivy Device in Post-radiation Patients

Status Not yet recruiting

Clinical Trial Summary

The objective of this study is to evaluate the feasibility of using the Hyivy device as a non-hormonal therapy in post-radiation patients with pelvic malignancies

Clinical Trial Description

Prior to study enrollment, all prospective participants will have the ability to contact the study team to learn more about the study and be provided with the relevant study-specific information. After being informed about the study and potential risks, all participants giving written informed consent will be assessed for their eligibility for the study, and enrolled participants will undergo a maximum 30-day screening period. On Day 0, eligible participants will start a 12-week use of Hyivy device with one visit on Week 6-7 and another on Week 12. After completing the 12-week intervention period, a virtual follow-up will be conducted on Week 16. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05648253
Study type	Interventional
Source	Hyivy Health Inc
Contact	Sabrina Collins, BSc
Phone	(519) 749-4370
Email	Sabrina.collins@grhosp.on.ca
Status	Not yet recruiting
Phase	N/A
Start date	June 30, 2024
Completion date	December 31, 2025

View Details

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