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

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

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCTs062220057

Enrollment

Registered

2022-09-21

Start date

2023-07-27

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate cancer, Bladder cancer

Interventions

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

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Postoperative erectile dysfunction in patients olde r than 40 years.

Exclusion criteria

Exclusion criteria: Non-neuropreserved cases, cases over 75 years ol d40

Design outcomes

Primary

Measure	Time frame
IIEF-6	—

Secondary

Measure	Time frame
Index of Erectile Dysfunction 15 Erection Hardnes s Score Masturbation Erection Index Number of urinary in continence pads IPSS OABSS AIS Evaluate before and after PGE1 injection Penile length and perimeter Blood flow velocity of corpus cavernosum Blood flow velocity of corpus cavernosum Blood flow velocity of dorsal penile artery Shear wave elastography of penis	—

Contacts

Public ContactKei Daizumoto

Tokushima university

daizumoto.kei@tokushima-u.ac.jp+81-886337159

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026