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NCT06483217 · ClinicalTrials.gov registry record · NA

Optimal Injection Interval for Intra-Detrusor Botulinum Toxin

A NA study, sponsored by Louisiana State University Health Sciences Center in New Orleans.

Not yet
Registry status
NA
Development phase
100
Enrollment target

NCT06483217 is a NA study that has not yet begun recruiting, run by Louisiana State University Health Sciences Center in New Orleans. The registered enrollment target is 100 participants.

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The verdict

NCT06483217, a NA study, has not yet begun recruiting, sponsored by Louisiana State University Health Sciences Center in New Orleans.

NOT YET RECRUITING
Registry status
NA
Development phase
100 participants
Enrollment target

Study Summary

The goal of this clinical trial is to see if patients deciding their own follow up times can increase the effectiveness of botulinum toxin (BTX or "Botox") injection for overactive bladder (OAB). The main questions it aims to answer are: * Does the time between repeat injections differ from the 6-month standard when it is based on patient symptoms alone? * Does symptom control or patient satisfaction change when patients control their own follow up times? Participants will undergo standard botulinum toxin injection into the bladder for OAB treatment and will then be randomly assigned to follow up either at a standard 6-month interval or whenever they feel their symptoms return.

Interventions

  • BEHAVIORAL Patient-directed follow up

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2024-07
Est. Completion 2025-10
Phase NA

What the Registry Record Tells You About NCT06483217

The ClinicalTrials.gov registry entry for NCT06483217 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Louisiana State University Health Sciences Center in New Orleans, which has 45 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Patient-directed follow up is the first listed.

NCT06483217 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06483217 about?

NCT06483217 is a clinical study titled "Optimal Injection Interval for Intra-Detrusor Botulinum Toxin". The goal of this clinical trial is to see if patients deciding their own follow up times can increase the effectiveness of botulinum toxin (BTX or "Botox") injection for overactive bladder (OAB). The main questions it aims to answer are: * Does the time between repeat injections differ from the 6-m...

What is the current status of trial NCT06483217?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-07. Estimated completion is 2025-10.

What interventions are being tested in trial NCT06483217?

The interventions under investigation include: Patient-directed follow up (BEHAVIORAL).

Who is sponsoring clinical trial NCT06483217?

This trial is sponsored by Louisiana State University Health Sciences Center in New Orleans, which has 45 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.