RECRUITING

Double-S: a Wearable Device for Erectile Dysfunction

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to use a minimally invasive erectile device for patients suffering from erectile dysfunction.

Official Title

Double-S: a Wearable Device for Erectile Dysfunction

Quick Facts

Study Start:2024-03-21

Study Completion:2025-06

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05451563

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:MALE

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* males \>18 years old suffering from any cause moderate to severe erectile dysfunction (e.g. ED after radical prostatectomy and/or radiation therapy for prostate cancer and or other pelvic malignancies affecting the sexual potency; emotional and psychological ED; organic vascular and/or metabolic ED etc.) * having a female partner willing to participate in the study	* not willing to attempt sexual vaginal intercourse with their partner * inability to wear/operate the external penile device for any reason

Contacts and Locations

Study Contact

Satvir Basran

CONTACT

650-723-0948

sbasran@stanford.edu

Principal Investigator

Michael Eisenberg, MD

PRINCIPAL_INVESTIGATOR

Stanford University

Study Locations (Sites)

Stanford Healthcare, Stanford Hospital

Stanford, California, 94304

United States

Collaborators and Investigators

Sponsor: Stanford University

Michael Eisenberg, MD, PRINCIPAL_INVESTIGATOR, Stanford University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-03-21

Study Completion Date2025-06

Study Record Updates

Study Start Date2024-03-21

Study Completion Date2025-06

Terms related to this study

Additional Relevant MeSH Terms

Erectile Dysfunction