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The influence of pelvic floor muscle training during 3 months in men, who still suffer from erectile dysfunction 12 months after open or robot radical prostatectomy: A randomised controlled trial.

The influence of pelvic floor muscle training during 3 months in men, who still suffer from erectile dysfunction 12 months after open or robot radical prostatectomy: A randomised controlled trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29363
Enrollment
40
Registered
2011-12-06
Start date
2011-05-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

prostate cancer, erectile dysfunction, open radical prostatectomy, robot radical prostatectomy, pelvic floor muscle exercises

Interventions

Patients, who still suffer from erectile dysfunction, 12 months after surgery, will be randomised in group 1 (starting immediately with pelvic floor muscle exercises) or in group 2 (starting 3 months

Sponsors

Katholieke Universiteit Leuven, Faculteit Bewegings- en Revalidatiewetenschappen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male patients, who had an unilateral/bilateral nervesparing open or robot radical prostatectomy at least 12 months earlier and still suffer from erectile dysfunction; 2. Patients who can participate in pelvic floor muslce training during the entire study period; 3. Patients who are willing to quit additional medication, like PDE-5 inhibitors, intracavernous injections during the entire study period.

Exclusion criteria

Exclusion criteria: 1. Patients, who didn't have erections and/or sexual intercourse preoperatively; 2. Patients, who underwent a nonnerve sparing radical prostatectomy; 3. Patients , who are not willing to quit additional medication, like PDE-5 inhibitors, intracavernous injections during the entire study period; 4. Patients, who are not able to perform pelvic floor muscle exercises because of cognitive problems; 5. Patients who refuse to participate in the study.

Design outcomes

Primary

MeasureTime frame
Improvement in erectile function: The patients will be evaluated by filling in the 'International Index of Erectile Function- Questionnaire' and the 'Erectile Hardness Scale' at several time points.

Secondary

MeasureTime frame
At the same time points the patient and his partner will be interviewed concerning the quality of the erection, orgasm and relation.

Contacts

Public ContactInge Geraerts

Postbus 1501

inge.geraerts@faber.kuleuven.be+32 16329120

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)