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Penile Rehabilitation with Vacuum Erectile Device following Robotic-assisted Radical Prostatectomy

Penile Rehabilitation with Vacuum Erectile Device following Robotic-assisted Radical Prostatectomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20191007003
Enrollment
Unknown
Registered
2019-10-07
Start date
2018-02-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Erectile dysfunction following robotic&#45

Interventions

One month after surgery&#44
patients in Study group will be instructed to use VED without constriction ring for 10 minutes every day continuously for six months,No additional penile rehabilitation device will be applied to Contr
Active Comparator Device,No Intervention No treatment
Vacuum erectile device (VED),Control

Sponsors

None listed

Eligibility

Sex/Gender
Male
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with localized prostate cancer and will undergo robotic-assisted radical prostatectomy 2. Sexually active and able to obtain a partial or full erection

Exclusion criteria

Exclusion criteria: 1. Severe erectile dysfunction defined by having an IIEF-5 score of less than 12 2. Penile curvature 3. History of priapism 4. Bleeding disorder

Design outcomes

Primary

MeasureTime frame
Erectile function Baseline, 1 month, 4 month, 7 month IIEF-5 score—

Secondary

MeasureTime frame
Penile length Baseline, 1 month, 4 month, 7 month Stretched penile length,Penile girth Baseline, 1 month, 4 month, 7 month Midshaft circumference—

Countries

Thailand

Contacts

Public ContactManint Usawachintachit

King Chulalongkorn Memorial Hospital

manint.u@chula.ac.th+66820902777

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026