Shock Wave vs. On-demand Tadalafil for Erectile Dysfunction
Primary Purpose
Erectile Dysfunction
Status
Recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
LI-ESWT
Tadalafil 20Mg Oral Tablet
Sponsored by
About this trial
This is an interventional treatment trial for Erectile Dysfunction focused on measuring Erectile dysfunction, Shock wave, Clinical trial
Eligibility Criteria
Inclusion Criteria:
- Male patients
- ED at least for 6 months
- vasculogenic ED
- from 25-60 years old
Exclusion Criteria:
- psychological patents
- neurological patients
- younger than 25 years old
- older than 60 years old
Sites / Locations
- Menoufia UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Shockwave group
Medical Treatment Group
Arm Description
This group will receive 6 sessions (2 per week) with average 6,000 shocks per session with the PiezoWave2 unit
This group will receive self-administered Tadalafil on-demand
Outcomes
Primary Outcome Measures
Erectile function assessed by International Index of Erectile Function-5
We will asessess erectile function using International Index of Erectile Function-5 (IIEF-5) where scores ≤6, severe; 8-16, moderate; 17-21, mild; and 22-25, none.
Secondary Outcome Measures
Erection hardness score
We will assess the Erection Hardness Score (EHS) was based on self-estimated rigidity, categorized using a scale of 1- 4: (1) the penis is larger but not hard, (2) the penis is hard but not hard enough for penetration, (3) the penis is hard enough for penetration but not completely hard, and (4) the penis is completely hard and fully rigid for coitus
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05199727
Brief Title
Shock Wave vs. On-demand Tadalafil for Erectile Dysfunction
Official Title
Comparison of the Efficacy and Safety of Low Intensity Extracorporeal Shock Wave Therapy Versus On-demand Tadalafil for Erectile Dysfunction
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
March 2022 (Anticipated)
Study Completion Date
May 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Menoufia University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The objective of this study is to evaluate the effectiveness and safety of focused Li-ESWT on 25 participants complaining of ED compared to 25 participants complaining of ED on medical treatment on a prospective clinical trial for 12 weeks.
Detailed Description
Penile erection is a very complex process which requires a delicate and coordinated equilibrium among the neurological, vascular and the tissue compartments. It also includes arterial dilation, trabecular smooth muscle relaxation, and activation of the corporeal veno occlusive mechanism.Erectile dysfunction is defined as persistent inability to achieve or maintain the erection that is sufficient to permit satisfactory sexual intercours. It has a multifactorial pathogenesis, one of them is vasculogenic ED that occurs due to diseases such as diabetes mellitus, hypertension, hyperlipidemia, smoking, or vascular occlusive disease.
ED is also the most commonly treated sexual disorder and it affects approximately 20% of adult males over the age of 20. Nowadays, there are several treatment solutions for patients with ED, either non-invasive or invasive but the phosphodiesterase 5 inhibitors are still the first-line therapy for ED.
However, PDE5-Is effect is limited due to their inability to improve penile blood flow for a time period that is sufficient to allow optimal oxygenation and recovery of Cavernosal vasculature. Also, they cannot improve spontaneous erections. Moreover, several patients ranging from 40% to 50% will not respond to drug therapy even after optimization approaches such as treatment combinations have been implemented.
Also, it was proven that the effect of long-term daily use of PDE5-Is on endothelial function has induced a short-term improvement in erectile function but probably not a longstanding one.
Another option for ED patients is the use of intracavernosal injections which is considered the second line of treatment. Although PDE5-Is and intracavernosal injections are effective and safe vasodilating agents, they are unable to alter the underlying predominant pathology in patients with vasculogenic ED (eg, cavernosal artery insufficiency).
Other options include the use of intraurethral injections, or vacuum constrictive devices that could serve as salvage therapy for patients who failed to respond to PDE5-Is. If the previous options failed or not preferred by the patient, penile prosthesis implantation would be the last resort treatment for ED.
Many trials were done to find a new treatment modality that would provide a rehabilitative or curative effect for ED. This modality should affect the endothelial function and improve penile hemodynamics. One of these modalities was low-intensity extracorporeal shockwave therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Erectile Dysfunction
Keywords
Erectile dysfunction, Shock wave, Clinical trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Shockwave group
Arm Type
Experimental
Arm Description
This group will receive 6 sessions (2 per week) with average 6,000 shocks per session with the PiezoWave2 unit
Arm Title
Medical Treatment Group
Arm Type
Active Comparator
Arm Description
This group will receive self-administered Tadalafil on-demand
Intervention Type
Device
Intervention Name(s)
LI-ESWT
Other Intervention Name(s)
Shockwave therapy
Intervention Description
Low intenisty shockwave therapy newly used for treatment of erectile dysfunction by applying 6 sessions on 3 weeks (2 sessions /week)
Intervention Type
Drug
Intervention Name(s)
Tadalafil 20Mg Oral Tablet
Intervention Description
Patients on this arm will allocate on on-demand tadalafil 20 mg for treatment of ED
Primary Outcome Measure Information:
Title
Erectile function assessed by International Index of Erectile Function-5
Description
We will asessess erectile function using International Index of Erectile Function-5 (IIEF-5) where scores ≤6, severe; 8-16, moderate; 17-21, mild; and 22-25, none.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Erection hardness score
Description
We will assess the Erection Hardness Score (EHS) was based on self-estimated rigidity, categorized using a scale of 1- 4: (1) the penis is larger but not hard, (2) the penis is hard but not hard enough for penetration, (3) the penis is hard enough for penetration but not completely hard, and (4) the penis is completely hard and fully rigid for coitus
Time Frame
3 months
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Male patients
ED at least for 6 months
vasculogenic ED
from 25-60 years old
Exclusion Criteria:
psychological patents
neurological patients
younger than 25 years old
older than 60 years old
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
HOSAM KOTB, master
Phone
01022707580
Email
hosam.kotb2020@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
fouad zanaty, professor
Organizational Affiliation
Menoufia University
Official's Role
Study Director
Facility Information:
Facility Name
Menoufia University
City
Cairo
ZIP/Postal Code
32632
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Menoufia University
Phone
048 2222170
Email
irbmnf@mnf.edu.eg
12. IPD Sharing Statement
Citations:
PubMed Identifier
31027441
Citation
Dong L, Chang D, Zhang X, Li J, Yang F, Tan K, Yang Y, Yong S, Yu X. Effect of Low-Intensity Extracorporeal Shock Wave on the Treatment of Erectile Dysfunction: A Systematic Review and Meta-Analysis. Am J Mens Health. 2019 Mar-Apr;13(2):1557988319846749. doi: 10.1177/1557988319846749.
Results Reference
background
PubMed Identifier
27986492
Citation
Clavijo RI, Kohn TP, Kohn JR, Ramasamy R. Effects of Low-Intensity Extracorporeal Shockwave Therapy on Erectile Dysfunction: A Systematic Review and Meta-Analysis. J Sex Med. 2017 Jan;14(1):27-35. doi: 10.1016/j.jsxm.2016.11.001. Epub 2016 Dec 13.
Results Reference
background
PubMed Identifier
32216245
Citation
Mo DS, Zhan XX, Shi HW, Cai HC, Meng J, Zhao J, Shang XJ. [Efficacy and safety of low-intensity extracorporeal shock wave therapy in the treatment of ED: A meta-analysis of randomized controlled trials]. Zhonghua Nan Ke Xue. 2019 Mar;25(3):257-264. Chinese.
Results Reference
background
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Shock Wave vs. On-demand Tadalafil for Erectile Dysfunction
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