The Treatment Efficacy of Prolotherapy in Bladder Voiding Dysfunction

Sponsor
Taichung Armed Forces General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05485142
Collaborator
(none)
80
1
2
50
1.6

Study Details

Study Description

Brief Summary

Voiding dysfunction including overactive bladder, underactive bladder, and neuropathic bladder. Voiding dysfunction has a great impact on life quality, especially in the elderly society. The current medication for overactive bladder has limited efficacy and the patient easily to dropout the medication because of its side-effects. The underactive bladder is a new entity of voiding dysfunction, its optimal is still unknown. Sacral neuromodulation(SNM) and posterior tibial nerve stimulation(PTNS) have been applied for both overactive bladder and underactive bladder treatment and the results is promising, but the equipment of SNM or PTNS is not available in most places. Prolotherapy using glucose local injection causing inflammatory reaction to stimulate cytokine and growth factors release. Investigators combined the concepts of posterior tibial nerve stimulation and prolotherapy to treat voiding dysfunction. Investigators anticipate it maybe a new promising treatment for voiding dysfunction.

Condition or Disease Intervention/Treatment Phase
  • Procedure: prolotherapy
N/A

Detailed Description

Inclusion criteria:1. Adults over 20 years-old. 2. The patient who meets the diagnostic criteria of overactive bladder or underactive bladder. 3. The patient who capable to complete 3-days voiding diary and the questionnaire. Exclusion criteria: 1. The patient has severe stress urinary incontinence, severe pelvic organ prolapse, acute urinary tract infection, urolithiasis, or urinary tract malignancy. 2. The patient who has active skin disease on legs or not suitable for leg local injection. 3. Pregnant women. Method: 40 overactive bladder patients and 40 underactive bladder patients. The patients will receive 5% glucose 10ml local injection peripheral to posterior tibial nerve near ankle under ultrasound guidance once a week for 4 weeks, then the patients will be followed up once-a-month for 3 months. OverActive Bladder Symptom Score(OABSS), Core Lower Urinary Tract Symptom score(CLSS) questionnaire, 3-days voiding diary, and urine nerve growth factor are used for assessment.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Treatment Efficacy of Prolotherapy in Bladder Voiding Dysfunction
Actual Study Start Date :
May 1, 2019
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: overactive bladder

Overactive bladder

Procedure: prolotherapy
5% glucose 10ml local injection peripheral to posterior tibial nerve near ankle under ultrasound guidance once a week for 4 weeks.

Experimental: Underactive bladder

Underactive bladder

Procedure: prolotherapy
5% glucose 10ml local injection peripheral to posterior tibial nerve near ankle under ultrasound guidance once a week for 4 weeks.

Outcome Measures

Primary Outcome Measures

  1. Overactive Bladder Symptom Score [Week 0]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

  2. Overactive Bladder Symptom Score [Week1]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

  3. Overactive Bladder Symptom Score [Week2]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

  4. Overactive Bladder Symptom Score [Week3]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

  5. Overactive Bladder Symptom Score [Week4]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

  6. Overactive Bladder Symptom Score [Week8]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

  7. Overactive Bladder Symptom Score [Week12]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

  8. Overactive Bladder Symptom Score [Week16]

    The improvement of overactive bladder symptom score (OABSS), OABSS ranged from 0 to 15, the higher score means more severity of overactive bladder.

Secondary Outcome Measures

  1. Cystometric bladder capacity [Week0]

    Cystometric bladder capacity: the volume of water instilled into bladder while performing cystometry examination.

  2. Cystometric bladder capacity [Week4]

    Cystometric bladder capacity: the volume of water instilled into bladder while performing cystometry examination.

  3. Cystometric bladder capacity [Week16]

    Cystometric bladder capacity: the volume of water instilled into bladder while performing cystometry examination.

Other Outcome Measures

  1. The improvement of Patient Perception of Bladder Condition (PPBC) [Week 0]

    The PPBC measures the patients' perception of their urinary (bladder) problems. Ranged from 1 to 6. The core 1 means no bother from bladder condition, higher score means more bother form bladder condition.

  2. The improvement of Patient Perception of Bladder Condition [Week1]

    The PPBC measures the patients' perception of their urinary (bladder) problems. Ranged from 1 to 6. The core 1 means no bother from bladder condition, higher score means more bother form bladder condition.

  3. The improvement of Patient Perception of Bladder Condition [Week2]

    The PPBC measures the patients' perception of their urinary (bladder) problems. Ranged from 1 to 6. The core 1 means no bother from bladder condition, higher score means more bother form bladder condition.

  4. The improvement of Patient Perception of Bladder Condition [Week3]

    The PPBC measures the patients' perception of their urinary (bladder) problems. Ranged from 1 to 6. The core 1 means no bother from bladder condition, higher score means more bother form bladder condition.

  5. The improvement of Patient Perception of Bladder Condition [Week4]

    The PPBC measures the patients' perception of their urinary (bladder) problems. Ranged from 1 to 6. The core 1 means no bother from bladder condition, higher score means more bother form bladder condition.

  6. The improvement of Patient Perception of Bladder Condition [Week8]

    The PPBC measures the patients' perception of their urinary (bladder) problems.

  7. The improvement of Patient Perception of Bladder Condition [Week12]

    The PPBC measures the patients' perception of their urinary (bladder) problems. Ranged from 1 to 6. The core 1 means no bother from bladder condition, higher score means more bother form bladder condition.

  8. The improvement of Patient Perception of Bladder Condition [Week16]

    The PPBC measures the patients' perception of their urinary (bladder) problems. Range from 1 to 6. The core 1 means no bother from bladder condition, higher score means more bother form bladder condition.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Adults over 20 years-old.

  2. The patient who meets the diagnostic criteria of overactive bladder or underactive bladder.

  3. The patient who capable to complete 3-days voiding diary and the questionnaire.

Exclusion Criteria:
  1. Severe stress urinary incontinence or severe pelvic organ prolapse.

  2. Acute urinary tract infection.

  3. Active hematuria, urolithiasis, or neoplasm of urinary tract.

  4. Acute skin lesion over the ankle injection site or the patient who could not tolerate ankle injection.

  5. Pregnant women.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Taichung Armed Forces General Hospital Taichung Other (Non US) Taiwan 41168

Sponsors and Collaborators

  • Taichung Armed Forces General Hospital

Investigators

  • Principal Investigator: Jing-dung Shen, Taichung Armed Forces General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jing-Dung, SHEN, Senior Urologist, Taichung Armed Forces General Hospital
ClinicalTrials.gov Identifier:
NCT05485142
Other Study ID Numbers:
  • 108B01
First Posted:
Aug 3, 2022
Last Update Posted:
Aug 3, 2022
Last Verified:
Jul 1, 2022
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
Keywords provided by Jing-Dung, SHEN, Senior Urologist, Taichung Armed Forces General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 3, 2022