Erectile dysfunction erection dysfunction
Conditions
Interventions
None listed
Sponsors
Sint Antonius Ziekenhuis
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: Healthy volunteer without (a history of) erectile dysfunction Male Aged 18 - 29 years
Exclusion criteria
Exclusion criteria: Test subjects who are unwilling to sign informed consent Test subjects with erectile dysfunction IIEF-5 score of below 17 (History of) sickle cell aneamia, atherosclerosis and diabetes type I or II. (History of) REM-sleep behavior disorder or other sleep disorders such as restless legs syndrome, insomnia, and sleep apnea Usage of sleeping pills or benzodiazepines.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main endpoint of the Feeling Hot 2 study is to determine the change in penile skin temperature and increased duration of (de)tumescence during nocturnal erections. With these outcomes, the validity of temperature measurements to detect nocturnal erections can be determined. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome of the Feeling Hot 2 study combines the results of the Feeling Hot 1 study. It is studied what differences in bodily skin temperature exist between nocturnal erections and visually aroused erections. Furthermore, it is studied whether the reference temperature probe placed on the outer thigh can compensate for the environmental influences of blankets and clothing. | — |
Countries
Netherlands
Outcome results
None listed