A prospective study on the efficacy of rehabilitation using TENGA for postoperative erectile dysfunction

JRCT ID: jRCTs062220057

Registered date:21/09/2022

Basic Information

• Recruitment status: Pending
• Health condition(s) or Problem(s) studied: Prostate cancer, Bladder cancer
• Date of first enrollment: 21/09/2022
• Target sample size: 30
• Study type: Interventional
• Intervention(s): The control group will receive normal medical car e and no rehabilitation. The intervention group wil l undergo rehabilitation using a combination of the TENGA Healthcare Men's Training Cup and the TE NGA Vacuum Controller for 30 minutes three time s a week.

Outcome(s)

• Primary Outcome: IIEF-6

Secondary Outcome

Index of Erectile Dysfunction 15 Erection Hardnes s Score
Masturbation Erection Index Number of urinary in continence pads
IPSS OABSS
AIS
Penile length
Blood flow velocity of corpus cavernosum
Blood flow velocity of corpus cavernosum
Blood flow velocity of dorsal penile artery
Shear wave elastography of penis

Key inclusion & exclusion criteria

• Age minimum: >= 40age old
• Age maximum: < 75age old
• Gender: Male
• Include criteria: Postoperative erectile dysfunction in patients olde r than 40 years.
• Exclude criteria: Non-neuropreserved cases, cases over 75 years ol d40

Related Information

• Primary Sponsor: Daizumoto Kei
• Source(s) of Monetary Support: Tenga Healthcare Co.