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Clinical Trials/NCT05337813
NCT05337813UnknownNot Applicable

Effects of Low-intensity Excoporeal Shock Wave Therapy (LiESWT) on Women With Pelvic Floor Dysfunction

Kaohsiung Medical University Chung-Ho Memorial Hospital1 site in 1 country120 target enrollmentStarted: April 10, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
120
Locations
1
Primary Endpoint
Reduce bladder leakage and symptoms of overactive bladder, including urgency, incontinence and nocturia.

Study Overview

Brief Summary

  1. This study needles female reproductive urinary tract, likely bladder hyperactivity, active urinary incontinence and interstitial cystitis, observation use of low-capacity seismic wave (LiESWT) therapy combined with combined platelet plasma (PRP), improved bone basin pain and female Urinary incontinence.
  2. LiESWT to arousal the clitoris angiogenesis to prevent female sexual dysfunction.

Detailed Description

Collect 120 women(A. Overactive bladder、B. Stress incontinence、C. Interstitial cystitis D. Female sexual dysfunction), Low Energy Extracorporeal Shock Wave (LiESWT) therapy once a week, duration 8 weeks(B.、C. PRP treatment at 1, 5, 9 weeks), and to complete all treatment after 4 weeks and 24 weeks back to the clinic, evaluation questionnaire (OABSS、UDI-6、IIQ-7、ICIQ-SF、POPDI-6、FSFI)、Urinary tract dynamics test、Urination log、Cotton pad test、Blood test(ESR、CA125、CBC、CRP). ○DLow Energy Extracorporeal Shock Wave (LiESWT) therapy once a week, duration 4 weeks, and to complete all treatment 4th and after 4 weeks back to the clinic, Pelvic Doppler ultrasound ,evaluation questionnaire (OABSS、UDI-6、IIQ-7、ICIQ-SF、POPDI-6、FSFI).

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to 99 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •One of the following symptoms can be included:
  • •Overactive bladder
  • •Stress incontinence
  • •Interstitial cystitis
  • •Not Menopause and female sexual dysfunction (FSFI scores< 26)
  • •The blood test confirmed that the number of platelets was 150,000 to 450,000 / UL, and the coagulation function (PT) index was normal.
  • •Women over 20 years.

Exclusion Criteria

  • •No UTI during the past week.
  • •Patients with poorly controlled diabetes, spinal cord injury, brain disease and neurogenic disease.
  • •urinary symptoms of inflammation(Bladder stones、hematuria、urethral syndrome).
  • •Patients with acute or chronic infectious diseases.
  • •Patients with acute or chronic cardiovascular disease.
  • •Patients with a history of chronic liver and kidney disease.
  • •Patients receiving anticoagulant therapy(Aspirin and NSAIDs COX-1).
  • •Patients with bleeding disorders.
  • •Receive low energy extracorporeal shock wave treatment within 1 month before entering the trial.
  • •Urinary incontinence need to install the catheter.
  • •Pregnant women.
  • •Unable to sign the consent form.

Arms & Interventions

A. Overactive bladder

Experimental

Overactive bladder (LiESWT therapy once a week, duration 8 weeks)

Intervention: "Storz Medical" Extracoporeeal Shock Wave Therapy System (Device)

B. Stress incontinence

Experimental

Stress incontinence (LiESWT therapy once a week, duration 8 weeks + PRP therapy once a month, duration 3 months)

Intervention: "Storz Medical" Extracoporeeal Shock Wave Therapy System (Device)

C. Interstitial cystitis

Experimental

Interstitial cystitis (LiESWT therapy once a week, duration 8 weeks + PRP therapy once a month, duration 3 months)

Intervention: "Storz Medical" Extracoporeeal Shock Wave Therapy System (Device)

D. Female sexual dysfunction

Experimental

Female sexual dysfunction (LiESWT therapy once a week, duration 8 weeks)

Intervention: "Storz Medical" Extracoporeeal Shock Wave Therapy System (Device)

Outcomes

Primary Outcomes

Reduce bladder leakage and symptoms of overactive bladder, including urgency, incontinence and nocturia.

Time Frame: 8 months

1.Questionnaire assessment before and after treatment (OABSS, UDI-6, IIQ-7, ICIQ-SF, POPDI-6, FSFI) . 2.urodynamic examination before and after treatment

Assess the patient for changes in lower abdominal pain

Time Frame: 8 months

VAS pain index record before and after treatment

Secondary Outcomes

  • Promote the repair and proliferation of blood vessels in the vulva to improve sexual function and improve the overall quality of sexual life.(2 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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