Clinical Trials Logo

Clinical Trial Summary

This study is a unique one as it si done for first time to all patients following bladder injury in PAS surgery. Bladder function will be assessed by urodynamic study.


Clinical Trial Description

Patients will be initially assessed by overactive bladder (OAB) and incontinence questionnaire. Examination was done to determine any neurological, or congenital abnormalities. Urodynamic study (UDS) will done for all patients. The patients will be asked to drink fluids to obtain a comfortably full bladder. Initially, a pelvic-abdominal ultrasound was done followed by the UDS. Urodynamic study consisted of uroflowmetry (volume: ≥150 ml and Qmax: 20-30 ml/s); filling cystometry in physiological or medium filling rate of 40 ml/min (using normal saline at room temperature through a double lumen urethral catheter); stress leak test; and pressure flow study. No sedation will be administered during the study as the patient should be aware. The patients were placed in a semi-seated lithotomy position. After a detailed explanation to the patient, the examination will begin by passing a catheter into the bladder (5 Fr) to measure the postvoiding residual urine followed by filling the bladder and measuring the intravesical pressure through the catheter. A rectal catheter was placed for measuring the abdominal pressure. The systems will be always zeroed at the atmospheric pressure. The patients will be periodically asked to cough to check the operation of the equipment and instructed to report her sensations. The volume of the first sensation of filling, first desire (1 s) and second desire (2 s) were recorded. When the bladder was filled up to 150 ml, patients were asked to cough (Valsalva) to predict the stress leakage. If not occur at 150 ml, the bladder was refilled, and the stress test was repeated until the leakage occurred or the bladder capacity was reached. Additionally, any unidentified involuntary detrusor contractions will be noted. When the patient had the urge to void, the permission for voiding will be given. Then voiding cystometrogram (pressure-flow) was performed and the urodynamic parameters, such as maximum flow rate (Qmax) and detrusor pressure at maximum flow (Pdet Qmax) will be observed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04835766
Study type Observational
Source Tanta University
Contact Ayman Dawoog, MD
Phone +202020972067
Email ayman.dawood@med.tanta.edu.eg
Status Recruiting
Phase
Start date July 1, 2021
Completion date July 31, 2024

See also
  Status Clinical Trial Phase
Withdrawn NCT00713921 - Neuropathic Investigation and Anticholinergic Treatment of Bladder Dysfunction in Diabetes and Stroke Patients Early Phase 1
Withdrawn NCT00472784 - Quantitative and Qualitative Changes in Neural Efferent Receptors
Completed NCT04528784 - Feasibility Study of Transcutaneous Tibial Nerve Stimulation for Urinary Symptoms in People With Multiple Sclerosis N/A
Completed NCT02910596 - Effectiveness of Bethanechol Chloride and Early Bladder Training for Prevention of Bladder Dysfunction After Radical Hysterectomy in Cervical Cancer Stage IB - IIA Phase 4
Terminated NCT00688948 - Alfuzosin for Voiding Dysfunction in Multiple Sclerosis (MS) Phase 2/Phase 3
Completed NCT05858840 - Urinary Artificial Sphincter in Children
Recruiting NCT05968352 - Restoration of Bladder Function in Spinal Cord Injury
Recruiting NCT05462561 - Vascularized Composite Bladder Allograft Transplantation N/A
Completed NCT05013541 - Effect of Bladder Filling on Rectal Contractions During Cystometry
Recruiting NCT04993859 - Impact of Chemotherapy on Urinary Biomarkers and Non-Invasive Urodynamics in Children
Recruiting NCT04626167 - Concomitant Renal and Urinary Bladder Allograft Transplantation Early Phase 1
Completed NCT03570593 - Removal of Urinary Catheter After Radical Surgery N/A
Active, not recruiting NCT04490642 - Linguistic Validation of the Childhood Bladder and Bowel Dysfunction Questionnaire (CBBDQ) for 5-12 Years Old in Korean
Completed NCT04057222 - Effect of Need to Void on Rectal Sensory Function in Multiple Sclerosis
Completed NCT05351138 - Comparison of Transcutaneous Electrical Nerve Stimulation and Manual Therapy in Children With Cerebral Palsy N/A
Completed NCT03987126 - Prebiotics for Spinal Cord Injury Patients With Bowel and Bladder Dysfunction Phase 3
Completed NCT01460303 - Patient-operated Valved Catheter Versus Indwelling Transurethral Catheter N/A
Completed NCT00280592 - Cranberry for Prevention of Urinary Tract Infections in Multiple Sclerosis Patients Phase 3
Completed NCT05861011 - Bladder Neck Surgery in Children With Neurogenic Bladder
Completed NCT04134104 - Incidence of The Bowel, Bladder, and Sexual Dysfunction Following Surgery for Colorectal Malignancy