Trial · NCT03913819
Treatment Outcomes Under a Standardized Treatment Protocol in Patients Suffered Substance Abuse Related Voiding Dysfunction
NCT03913819, Recruiting, Chinese University of Hong Kong
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Treatment Outcomes Under a Standardized Treatment Protocol in Patients Suffered Substance Abuse Related Voiding Dysfunction. Trials, record NCT03913819. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03913819
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Treatment Outcomes Under a Standardized Treatment Protocol in Patients Suffered Substance Abuse Related Voiding Dysfunction
- NCT number
- NCT03913819
- Status
- Recruiting
- Enrollment
- 1,500 participants, estimated
- Lead sponsor
- Chinese University of Hong Kong
- Conditions
- Voiding Dysfunction, Substance Abuse
- Interventions
First line treatment: oral NSAID and anticholinergic agents, Second line treatment: additional treatment for pain control, Third line treatment: A course of intravesical hyaluronate will be given., Fourth line treatment: surgical intervention
- First posted
- 2019-04-12
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in total Bladder Capacity after standardized treatment. | Baseline, 4 months, 8 months, 12 months, every 4 months through study completion, and average of 1 year | Total bladder capacity is assessed by the sum of voided volume and post-voided volume |
| Primary | Change in Pain level after standardized treatment: Pelvic Pain - Urgency Frequency symptom scale | Baseline, 4 months, 8 months, 12 months, every 4 months through study completion, and average of 1 year | Using the Pelvic Pain - Urgency Frequency symptom scale |
| Primary | Change in Bladder storage function after standardized treatment | Baseline, 4 months, 8 months, 12 months, every 4 months through study completion, and average of 1 year | Using Overactive Bladder Symptom Score |
| Primary | Change in Bladder voiding function after standardized treatment | Baseline, 4 months, 8 months, 12 months, every 4 months through study completion, and average of 1 year | Using the International Prostate Symptom Score |
| Primary | Any new Adverse events related to treatment modalities | Baseline, 4 months, 8 months, 12 months, every 4 months through study completion, and average of 1 year | By patient reporting |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers6
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03913819
GET https://conductscience.org/api/trials/v1/NCT03913819/registered