Voiding Dysfunction Clinical Trial
— DACOfficial title:
A New Approach to Clinical Implication of Detrusor After-contraction (DAC)
Verified date | June 2010 |
Source | Seoul National University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Korea: Institutional Review Board |
Study type | Observational |
The aims of this study are
- to confirm whether detrusor after-contraction (DAC) is a true contraction or not with a
new approach
- and to understand clinical implication of DAC
Status | Completed |
Enrollment | 2309 |
Est. completion date | December 2008 |
Est. primary completion date | December 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Indications and selection of patients for conduction of urodynamic studies (UDS) were followed as the recommendation of ICS (international continence society). Exclusion Criteria: - Patients with indwelling catheters, urinary tract infection and urinary stones were excluded from this study |
Observational Model: Case Control, Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul National University Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Hospital |
Korea, Republic of,
Ruarte AC, Podestá ML, Medel R. Detrusor after-contractions in children with normal urinary tracts. BJU Int. 2002 Aug;90(3):286-93. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | to confirm whether DAC is a true contraction or not | no change of Pdet when patients cough could confirm that DAC was a true contraction. Because an artifact occurred when a catheter was pressed against bladder wall or urethra, no change of intravesical pressure and increase of abdominal pressure finally induced a negative deflection of Pdet and this change of Pdet could be regarded as an artifact. | up to 2 years (2007.Jan-2008.Dec) | No |
Secondary | Past medical history including neurological disorders and pelvic irradiation were also included in the database | One-way analysis of variance and the chi-square test were performed to determine whether there was a relationship between the presence of DAC and the underlying neurogenic and non-neurogenic conditions | up to 2 years (2007.Jan-2008.Dec) | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05439902 -
Efficacy of Alpha-blockers (Tamsulosin) in the Treatment of Symptomatic Dysuria in Multiple Sclerosis in Women
|
N/A | |
Terminated |
NCT00713908 -
Voiding Dysfunction in the Postoperative Period Following Placement of the TVT
|
N/A | |
Completed |
NCT00679315 -
Efficacy and Safety of Alfuzosin for the Treatment of Voiding Dysfunction in Female
|
Phase 2 | |
Completed |
NCT04010591 -
The Measurement of Bladder Impedance and Heart Rate During Urodynamic Study
|
||
Completed |
NCT00719589 -
Outcomes of Pudendal InterStim
|
N/A | |
Completed |
NCT01189136 -
Treatment for Acute Postoperative Voiding Dysfunction
|
N/A | |
Completed |
NCT00214045 -
Rigid Versus Flexible Cystoscopy in Women
|
N/A | |
Completed |
NCT05820139 -
Evaluating the Optimal Volume Voided for Passage of a Backfill-Assisted Voiding Trial Following Urogynecologic Surgery
|
N/A | |
Completed |
NCT03574610 -
Brain Targets in Patients With Bladder Emptying Difficulties
|
N/A | |
Recruiting |
NCT00839969 -
Cystoscopy Plus Urethral Dilatation Versus Cystoscopy Alone in Women With Overactive Bladder Syndrome and Impaired Voiding
|
N/A | |
Completed |
NCT01197248 -
Randomized Controlled Trial of Cystocele Plication Risks ("CPR Trial"): A Pilot Study
|
Phase 2 | |
Recruiting |
NCT03913819 -
Treatment Outcomes Under a Standardized Treatment Protocol in Patients Suffered Substance Abuse Related Voiding Dysfunction
|
||
Withdrawn |
NCT02297178 -
A Follow-net Investigation of a Randomised Study of Cystoscopy and Urethral Dilatation Versus Cystoscopy Alone in Women With Overactive Bladder Syndrome and Impaired Voiding
|
N/A | |
Not yet recruiting |
NCT06404996 -
Smart-phone Application Versus Conventional Paper for the Documentation of Voiding Dysfunction in Children
|
N/A | |
Completed |
NCT05295823 -
Patient Self Measurement of Post-Void Residual Bladder Volume (PVR) Using Ultrasound
|
N/A | |
Active, not recruiting |
NCT02193451 -
Urodynamics for Prostate Surgery Trial; Randomised Evaluation of Assessment Methods
|
N/A | |
Completed |
NCT01228370 -
Efficacy and Safety of Silodosin on Voiding Dysfunction Associated With Neurogenic Bladder
|
Phase 4 |