TRIP-patch vs Duplex

NCT ID: NCT06402097

Last Updated: 2024-05-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-06-05

Study Completion Date

2020-09-25

Brief Summary

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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

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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

Conditions

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Erectile Dysfunction

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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St. Antonius Hospital

OTHER

Sponsor Role lead

Responsible Party

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Evelien Trip

Study Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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St Antonius Hospital

Nieuwegein, Utrecht, Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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70945

Identifier Type: -

Identifier Source: org_study_id

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