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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06185218
Other study ID # KAEK/08.11.2023.530
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 2024
Est. completion date October 2024

Study information

Verified date February 2024
Source Basaksehir Cam & Sakura Sehir Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Botulinum toxin injection into the bladder is used in current practice in urological diseases such as overactive bladder or interstitial cystitis. As far as is known, botulinum toxin injection sites have not been clearly defined. In this study, investigators are planning to compare botulinum toxin effectiveness with different injection site maps.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date October 2024
Est. primary completion date October 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Older than 18 years - Interstitial cystitis patients - Overactive bladder Exclusion Criteria: - younger than 18 years

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intravesical Botulinum Toxin
Botulinum Toxin injections will be made into the bladder.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Basaksehir Cam & Sakura Sehir Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Overactive bladder-V8 questionnaire will be used for efficacy of treatment. The questionnaire contains 8 questions and every question may be scored between 0 and 5. Additionally, male gender get 2 points more. Therefore, a patient may be get between 0 and 42 points. More score means worse complaint. Estimated 1 month for every patient after treatment.
Primary Urodynamics test will be assessed for efficacy of treatment. Possible bladder contractions and residual volume will be measured in urodynamic testing to demonstrate effectiveness after treatment. The lack of pathological bladder contractions and normal residual urine mean better for patient and, show improving. Estimated 1 month for every patient after treatment.
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