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Penile Lengthening Pre-Penile Prosthesis Implantation

NCT03500406 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2020-01-06

Study results available
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Summary

This study is intended to utilize a novel, class I (ie. lowest risk, clinical studies not required) medical device to determine whether penile length can be increased in men prior to undergoing a penile prosthesis implantation procedure.

Conditions

Interventions

DEVICE

RestoreX

Penile traction therapy in the straight position

OTHER

Control

No treatment

Sponsors & Collaborators

Principal Investigators

  • Landon W Trost · Mayo Clinic

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-23
Primary Completion
2019-04-01
Completion
2019-04-01
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03500406 on ClinicalTrials.gov