Low-Intensity Extracorporeal Shockwave Therapy for Penile Rehabilitation in Post-Radical Prostatectomy Patients

Sponsor
Hospital Pengajar Universiti Putra Malaysia (Other)
Overall Status
Recruiting
CT.gov ID
NCT06076850
Collaborator
(none)
70
1
2
24
2.9

Study Details

Study Description

Brief Summary

Radical prostatectomy (RP) is one of the curative treatment modalities for localized or locally advanced prostate cancer. Urinary incontinence and erectile dysfunction (ED) are two most common complications after RP. Despite the advancement of prostate cancer treatment, ED post-RP remains a significant morbidity especially for patients who are sexually active pre-operatively. To improve the sexual function post-surgery, numerous strategies have been described including preservation of neurovascular bundles intra-operatively, post-operative physiotherapy, on-demand phosphodiesterase 5-inhibitors (PDE5i), regular PDE5i, intra-carvenosal injection or vacuum suction device.

Low-intensity extracorporeal shockwave therapy (LiESWT) is an emerging treatment modality of ED with promising result, and it is a well-established treatment of ED in patients with diabetes mellitus or vasculopathy. Most of the pre-clinical studies were done on post-RP ED rat models with bilateral cavernous nerve crush injury. LiESWT was observed to improve nerve-impaired ED significantly compared to sham procedures. There are currently one pilot study and one randomized controlled trial (RCT) published in the literature on this field. However, the published RCT was an open label study with no sham-controlled arm which could contribute to reporting bias and the treatment intensity might not be adequate. In our proposed study, we make a hypothesis that LiESWT and very early PDE5i can improve erectile function in patients after nerve-sparing radical prostatectomy.

Condition or Disease Intervention/Treatment Phase
  • Device: Low-Intensity Extracorporeal Shockwave Therapy (LiEWST) - Active
  • Device: Low-Intensity Extracorporeal Shockwave Therapy (LiEWST) - Sham
N/A

Detailed Description

Urinary incontinence and erectile dysfunction (ED) are two most common complications after RP. Despite the advancement of prostate cancer treatment, erectile dysfunction post-prostatectomy remains as a significant morbidity especially for patients who are sexually active pre-operatively. PDE5i such as Tadalafil, Sildenafil remains the main form of penile rehabilitation with limited success. Non-invasive treatment such as Li-ESWT has proven to be a good treatment option mainly for vasculogenic ED. This study aims to investigate the effect of Li-ESWT treatment on post-prostatectomy ED, along with regular PDE5i.

Our hypothesis is that Low intensity extracorporeal shockwave therapy and very early PDE5i can improve erectile function in patients after nerve-sparing post-radical prostatectomy.

Eligible patients will be randomized to intervention arm (LiESWT treatment for 6 weeks + Tadalafil 5mg daily for 12 months) or controlled arm (sham therapy for 6 weeks + Tadalafil 5mg daily for 12 months). The device used in this study is Dornier Aries 2, with treatment protocol as described. The vacuum pump is an option for penile rehabilitation protocol at our institution due to its expensive cost. Penile vacuum pumps are allowed for voluntary use by all participants in both groups. A sub-group analysis will be conducted at the conclusion of the study.

Sexual outcomes will be assessed using IIEF (International Index of Erectile Function), EHS (Erectile Hardness Score) and Erectile Dysfunction Inventory of Treatment Satisfaction Score (EDITS) questionnaires at 1,3,6 and 12 months after completion of therapy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Extracorporeal Shockwave Therapy for Penile Rehabilitation in Post-Radical Prostatectomy Patients: A Randomized, Double-Blinded, Sham-Controlled Study
Actual Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jun 30, 2025
Anticipated Study Completion Date :
Jun 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Standard Care + Active LiESWT

Tadalafil 5mg daily - to start 5 days before surgery and continued for 12 months after surgery till end of study. With or without Vacuum Pump Active LiESWT

Device: Low-Intensity Extracorporeal Shockwave Therapy (LiEWST) - Active
Treatment protocol: EFD 0.096 mJ/mm2 2 sessions / week; 5000 shocks / session 6 weeks treatment total: 12 sessions Li-ESWT to start after removal of indwelling catheter
Other Names:
  • Dornier Aries 2 (Dornier MedTech, Germany)
  • Sham Comparator: Standard Care + Sham LiESWT

    Tadalafil 5mg daily - to start 5 days before surgery and continued for 12 months after surgery till end of study. With or without Vacuum Pump Sham LiESWT

    Device: Low-Intensity Extracorporeal Shockwave Therapy (LiEWST) - Sham
    Treatment protocol: EFD 0 mJ/mm2 2 sessions / week; 5000 shocks / session 6 weeks treatment total: 12 sessions Li-ESWT to start after removal of indwelling catheter
    Other Names:
  • Dornier Aries 2 (Dornier MedTech, Germany)
  • Outcome Measures

    Primary Outcome Measures

    1. Sexual Function [12 months]

      Measurement of average change in IIEF-5 score from baseline (pre-RP) to specified time-points at 1,3,6 and 12 months after completion of treatment - 22-25: No erectile dysfunction 17-21: Mild erectile dysfunction 12-16: Mild to moderate erectile dysfunction 8-11: Moderate erectile dysfunction 5-7: Severe erectile dysfunction 5 being the worst outcome

    Secondary Outcome Measures

    1. Stretched Penile Length [12 months]

      Clinical measurement of change in stretched flaccid penile length from baseline specified time-points at 1,3,6 and 12 months after completion of treatment.

    2. Urinary Function [12 months]

      Measurement of average change in EPIC questionnaire score from baseline (pre-RP) to specified time-points at 1,3,6 and 12 months after completion of treatment.

    3. Safety and Adverse Events [12 months]

      Number of Participants With Treatment-Related Adverse Events as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) v5.0

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 75 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients who underwent radical prostatectomy (open, laparoscopic or robotic-assisted) with nerve-sparing (unilateral or bilateral).

    • Low / intermediate-risk prostate cancer

    • PSA < 20 ng/ml

    • Gleason score < 8

    • Prostate cancer pathological stage </= T2b

    • Sexually active with IIEF-5 score 3 18, with or without use of erectogenic aid / PDE5i.

    Exclusion Criteria:
    • Tumour upstaging beyond T2b

    • Neurovascular bundle tissues bilaterally in the histopathological report.

    • Scheduled treatment with pelvic radiotherapy and / or androgen deprivation therapy post-RP.

    • Men with ED of neuropathological, endocrine or psychogenic origin.

    • Previous pelvic surgery or radiation therapy.

    • Patients with uncontrolled psychiatric conditions.

    • Patients with major post-operative complications that could impact safety or effectiveness of ESWT.

    • Patients with heart disease - unable to take PDE5i or prohibited from sexual activity.

    • Patients on anticoagulation / antiplatelets except aspirin up to 100mg daily.

    • Inflammation in the shockwave area or having penile pathology such as Peyronie's disease.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital Sultan Abdul Aziz Shah, Universiti Putra Malaysia (previously known as HPUPM) Serdang Selangor Malaysia 43400

    Sponsors and Collaborators

    • Hospital Pengajar Universiti Putra Malaysia

    Investigators

    • Principal Investigator: Vincent Khor, ChM(Urol), Universiti Putra Malaysia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Hospital Pengajar Universiti Putra Malaysia
    ClinicalTrials.gov Identifier:
    NCT06076850
    Other Study ID Numbers:
    • JKEUPM-2023-073
    First Posted:
    Oct 11, 2023
    Last Update Posted:
    Oct 11, 2023
    Last Verified:
    Oct 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 11, 2023