Combined Treatment of Platelet-rich Plasma (PRP) and Low-intensity Extracorporeal Shockwave Therapy (Li-ESWT) on Erectile Dysfunction (ED)
Primary Purpose
Erectile Dysfunction
Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
autologous platelet-rich plasma and low-intensity extracorporeal shockwave therapy
Sponsored by
About this trial
This is an interventional treatment trial for Erectile Dysfunction focused on measuring erectile dysfunction, platelet-rich plasma, low-intensity extracorporeal shockwave therapy
Eligibility Criteria
Inclusion Criteria:
- Impotence for more than three months
- International index of erectile function, (IIEF) less than 21( including 21)
- Erectile hardness score, (EHS) less than 3( including 3)
- Age over 30 years old
Exclusion Criteria:
- Hypogonadism
- Bleeding tendency
- Could not cooperate with the treatment
- AIDS, syphilis and condyloma victim
- Received radical prostatectomy
- Prostate cancer or pelvis malignant tumor victim
- Gonad dysfunction
- Penis deformities
- Penile prosthesis implantation
- Psychiatric disease victim
- Neural disease ( multiple myeloma , brain atrophy, etc)
- Pacemaker implantation
- Not suitable join this trial judged by Investigator
- Alcohol or drug abuse
Sites / Locations
- Taipei Medical University HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
PRP and Li-ESWT treatment
Arm Description
Participants diagnosed with erectile dysfunction will receive the combined treatment of platelet-rich plasma and low-intensity extracorporeal shockwave therapy.
Outcomes
Primary Outcome Measures
The Change in Erectile Function
Using the International Index of Erectile Function (IIEF) questionnaire.
The Change in Erectile Function
Using the Erectile Hardness Scale (EHS) questionnaire to evaluate the efficacy of combined treatment of PRP and Li-ESWT
Secondary Outcome Measures
Incidents of Side Effects
To observe whether there are side effects
Full Information
NCT ID
NCT04416802
First Posted
June 2, 2020
Last Updated
October 4, 2022
Sponsor
Taipei Medical University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04416802
Brief Title
Combined Treatment of Platelet-rich Plasma (PRP) and Low-intensity Extracorporeal Shockwave Therapy (Li-ESWT) on Erectile Dysfunction (ED)
Official Title
A Clinical Study of the Combined Treatment of Platelet-rich Plasma and Low-intensity Extracorporeal Shockwave Therapy on Erectile Dysfunction
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 28, 2020 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
October 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Taipei Medical University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this clinical study is mainly to use platelet-rich plasma combined with low-intensity extracorporeal shockwave therapy to treat patients with erectile dysfunction and observe the improvement results.
Detailed Description
According to statistics from the Taiwan Society of Andrology, 18 to 25 years old male population in Taiwan having erectile dysfunction (ED) trouble is as high as 5 to 10 percent. At the same time, statistics from the Taiwan Sexual Dysfunction Counseling Training Committee show that as many as 50 percent of men between 40 and 70 years old have erectile dysfunction. Erectile dysfunction is the most common sexual dysfunction in men and is believed to be related to nerve or blood vessel damage, and often significantly affects the patients' quality of life.
PRP is the abbreviation of "platelet-rich plasma". It can release growth factors and cytokines in the body to further promote tissue repair. The results of pre-clinical and clinical trials show that PRP can promote the repair of cavernous tissue, protect erection function of nerve, and stimulate the regeneration of nerve.
Low-intensity extracorporeal shockwave therapy (Li-ESWT) is a non-invasive treatment. Under this treatment, it will help body producing angiogenesis-related proteins, stimulating the formation of small blood vessels, generating new blood vessels at the site to be treated, and increasing the perfusion flow of local tissues. Li-ESWT has been clinically shown to have a significant effect on erectile dysfunction.
The purpose of this clinical study is mainly to use platelet-rich plasma combined with low-intensity extracorporeal shockwave therapy to treat patients with erectile dysfunction and observe the improvement results.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Erectile Dysfunction
Keywords
erectile dysfunction, platelet-rich plasma, low-intensity extracorporeal shockwave therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
PRP and Li-ESWT treatment
Arm Type
Experimental
Arm Description
Participants diagnosed with erectile dysfunction will receive the combined treatment of platelet-rich plasma and low-intensity extracorporeal shockwave therapy.
Intervention Type
Combination Product
Intervention Name(s)
autologous platelet-rich plasma and low-intensity extracorporeal shockwave therapy
Intervention Description
The patient who encounters sexual dysfunction and visits our Outpatient Department (OPD) could enter this trial if he meets the inclusion criteria and exclusion criteria.
To fill the questionnaires of International index of erectile function (IIEF) and erectile hardness score (EHS) before starting treatment.
Li-ESWT treatment weekly for three weeks and PRP injection at the same day after the last Li-ESWT treatment.
Coming back at the fourth week and check is there any side effect and fill the questionnaires of IIEF and EHS.
Li-ESWT treatment weekly for three weeks starts on fifth week and PRP injection at the same day after the last Li-ESWT treatment.
Coming back at the eighth week and check is there any side effect and fill the questionnaires of IIEF and EHS.
Coming back at the twelfth week and check is there any side effect and fill the questionnaires of IIEF and EHS.
Primary Outcome Measure Information:
Title
The Change in Erectile Function
Description
Using the International Index of Erectile Function (IIEF) questionnaire.
Time Frame
Baseline, the 4th week, 8th week, and 12th weeks
Title
The Change in Erectile Function
Description
Using the Erectile Hardness Scale (EHS) questionnaire to evaluate the efficacy of combined treatment of PRP and Li-ESWT
Time Frame
Baseline, the 4th week, 8th week, and 12th weeks
Secondary Outcome Measure Information:
Title
Incidents of Side Effects
Description
To observe whether there are side effects
Time Frame
the 4th week, 8th week, and 12th weeks
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Impotence for more than three months
International index of erectile function, (IIEF) less than 21( including 21)
Erectile hardness score, (EHS) less than 3( including 3)
Age over 30 years old
Exclusion Criteria:
Hypogonadism
Bleeding tendency
Could not cooperate with the treatment
AIDS, syphilis and condyloma victim
Received radical prostatectomy
Prostate cancer or pelvis malignant tumor victim
Gonad dysfunction
Penis deformities
Penile prosthesis implantation
Psychiatric disease victim
Neural disease ( multiple myeloma , brain atrophy, etc)
Pacemaker implantation
Not suitable join this trial judged by Investigator
Alcohol or drug abuse
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ming-Che Liu, MD
Phone
886-2-2737-2181
Ext
1981
Email
d204097002@tmu.edu.tw
First Name & Middle Initial & Last Name or Official Title & Degree
Yi-Jen Su
Phone
886-2-2737-2181
Ext
5027
Email
175275@h.tmu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ming-Che Liu, MD
Organizational Affiliation
Taipei Medical University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Taipei Medical University Hospital
City
Taipei
ZIP/Postal Code
110
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ming-Che Liu, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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26500703
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Results Reference
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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Combined Treatment of Platelet-rich Plasma (PRP) and Low-intensity Extracorporeal Shockwave Therapy (Li-ESWT) on Erectile Dysfunction (ED)
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