Efficacy and Safety of Focused Shockwave Therapy Plus Tadalafil vs Tadalafil Alone in Patient With Erectile Dysfunction

Sponsor
Saint Petersburg State University, Russia (Other)
Overall Status
Recruiting
CT.gov ID
NCT05823506
Collaborator
(none)
36
1
2
12
3

Study Details

Study Description

Brief Summary

The goal of this trial is that using tadalafil plus low-intensity extracorporeal shockwave therapy (li-ESWT) is more effective than using tadalafil alone in improving erection rigidity and sexual function. The efficacy of the combination of li-ESWT and tadalafil has been confirmed by a number of studies, including in patients after radical prostatectomy. However, this method is still not a "first-line" method in young primary patients and its benefits in combination with drugs for these patients are not obvious.

We assume that the combination of tadalafil plus low-intensity extracorporeal shockwave therapy (li-ESWT) will improve the subjective state of patients assessed by points of validated questionnaires and Number of successful intercourse per week.

Condition or Disease Intervention/Treatment Phase
  • Combination Product: PDE5 inhibitor (tadalafil) and BTL-6000 fSWT
  • Drug: PDE5 inhibitor (tadalafil)
N/A

Detailed Description

The aim of the study is to test the hypothesis that using tadalafil plus shockwave in primary patient with ED treatment in more effective in improving erection rigidity and sexual function, then using tadalafil alone.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy and Safety of Focused Shockwave Therapy Plus Tadalafil vs Tadalafil Alone in Patient With Erectile Dysfunction: Randomized Controlled Trial
Actual Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Medication group

PDE5 inhibitor tadalafil in dosage 5 mg daily by 1 month

Drug: PDE5 inhibitor (tadalafil)
Tadalafil improves erectile function by inhibiting PDE5 isoenzyme, thereby blocking cGMP degradation. As a result, the PDE5 inhibitors act synergistically with NO to markedly increase the levels of cGMP, which in the presence of sexual stimulation, lead to an erection. In the absence of sexual stimulation, NO is not released locally and the PDE5 inhibitors do not affect the penis. Thus, sexual stimulation is needed to initiate the erectile mechanism for the PDE5 inhibitors to take effect.

Experimental: Combination group

PDE5 inhibitor tadalafil in dosage 5 mg daily by 1 month plus Device BTL-6000 fSWT: 6 sessions with EFD 0,09 mJ/mm2 by 5000 impulses per session in 5 points in corpora cavernosa penis

Combination Product: PDE5 inhibitor (tadalafil) and BTL-6000 fSWT
The mechanism of low-intensity shockwave therapy in patients with ED based on the effect on the endothelium of the cavernous arteries, the release of NO and the enhancement of vascularization due to release of angiogenic factors.

Drug: PDE5 inhibitor (tadalafil)
Tadalafil improves erectile function by inhibiting PDE5 isoenzyme, thereby blocking cGMP degradation. As a result, the PDE5 inhibitors act synergistically with NO to markedly increase the levels of cGMP, which in the presence of sexual stimulation, lead to an erection. In the absence of sexual stimulation, NO is not released locally and the PDE5 inhibitors do not affect the penis. Thus, sexual stimulation is needed to initiate the erectile mechanism for the PDE5 inhibitors to take effect.

Outcome Measures

Primary Outcome Measures

  1. IIEF-5 [60 days]

    IIEF-5 is validated erectile function assessment questionnaire. The possible scores for the IIEF-5 range from 5 to 25, with lower values representing poorer sexual function.

Secondary Outcome Measures

  1. PGI-I [14 days,30 days, 60days.]

    The Patient Global Imression of Improvement (PGI-I) is a global index that may be used to rate the response of a condition to a therapy. This is a transition scale that is a single question asking the patient to rate their urinary tract condition now, as compared with how it was prior to before beginning treatment on a scale from 1-Very much better to 7-Very much worse.

  2. Likert scale (7-point preferably) satisfaction questionnaire [14 days,30 days, 60days.]

    Likert Scale questions offer a range of answer options from either end of the spectrum for the respondents to choose from, where 1-extremely dissatisfied, 7- extremely satisfied

  3. Therapy comfort survey [14 days,30 days, 60days.]

    Modified scale indicating how comfort patients feel about therapy, where 1is totally uncomfortable, and 7 is very comfortable.

  4. Number of successful intercourse per week [14 days,30 days, 60days.]

    Number of successful intercourse per week

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 45 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No

Inclusion Criteria:• Age 20 to 45;

  • Married or have had a permanent sex partner for at least 3 months;

  • IIEF-5 questionnaire scores below 20

Exclusion Criteria:
  • History of previous use of PDE-5 inhibitors or fSWT;

  • Patients with diabetes mellitus;

  • Patients after the radical prostatectomy or major pelvic surgery;

  • Patients with a confirmed neurological disease that may have caused the ED (Multiple Sclerosis, Parkinson's Disease, spinal cord injury);

  • Patients with contraindications to the use of PDE-5 inhibitors and/or fSWT;

Contacts and Locations

Locations

Site City State Country Postal Code
1 SBPSU Saint Petersburg Russian Federation

Sponsors and Collaborators

  • Saint Petersburg State University, Russia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gleb Kovalev, The head of outpatient urology department, phD, Saint Petersburg State University, Russia
ClinicalTrials.gov Identifier:
NCT05823506
Other Study ID Numbers:
  • ESWT_tadalafil_in_ED
First Posted:
Apr 21, 2023
Last Update Posted:
Apr 21, 2023
Last Verified:
Apr 1, 2023
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 Apr 21, 2023