MedPath

TRIP-patch vs Duplex

Completed
Conditions
Erectile Dysfunction
Registration Number
NCT06402097
Lead Sponsor
St. Antonius Hospital
Brief Summary

To measure saturation and desaturation of the cavernosal tissue with a cutaneous placed penile sensor, before and during full rigidity. To validate discriminating sensor-readings between flaccid state and full rigidity of the penis

Detailed Description

To measure saturation and desaturation of the cavernosal tissue with a cutaneous placed penile sensor, before and during full rigidity. To validate discriminating sensor-readings between flaccid state and full rigidity of the penis

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
20
Inclusion Criteria
  • Indication for a penile duplex in our andrology clinic Signed informed consent Male Between 18-60 year
Exclusion Criteria
  • Patients who are unwilling to sign written informed consent
  • Patients unable to undergo a duplex of the penis
  • Patients with sickle cell anemia because this could affect the accuracy of the measurements

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
change in sensor-readings1 hour

To validate discriminating sensor-readings between flaccid state and full rigidity of the penis

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

St Antonius Hospital

🇳🇱

Nieuwegein, Utrecht, Netherlands

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