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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02665572
Other study ID # Zahran MH3182015
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 2015
Est. completion date October 2021

Study information

Verified date February 2021
Source Mansoura University
Contact Mohamed H Zahran, Dr
Phone 0502202638
Email zahranmha@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, investigators will prospectively evaluate the outcome of renal transplantation into a defunctionalized bladder by comparing direct transplantation into this defunctionalized bladder and pre-transplant programmed bladder cycling.


Description:

Study population: The study will include patients maintained on hemodialysis for more than 12 months, have oliguria or anuria, reduced bladder capacity, have no history of lower urinary tract dysfunction and have no evidence of urological cause of renal failure. Patients with history of lower urinary tract symptoms before developing renal failure and those with lower urinary tract disease resulting in renal failure will be excluded. Study design: It is a randomized controlled trial comparing the outcome of programmed bladder cycling before the time of renal transplantation and direct transplantation without bladder cycling in patients with defunctionalized bladder. Patients, who meet the inclusion criteria, will be randomly allocated into two groups. The first group will undergo renal transplantation on the defunctionalized bladder without bladder recycling. The second group will undergo renal transplantation after bladder recycling. Measurements: All patients will be diagnosed by proper history taking, cystoscopy, ascending cystogram and cystometry in order to confirm the diagnosis of reduced bladder capacity and exclude any organic or neurological cause. Bladder recycling will be done by the patient after proper education. It will be started by the instillation of the sterile water in the bladder in amount equal to the estimated bladder capacity. Then the amount will be gradually increased till the patient can withstand filling the bladder with 300 cc of sterile water for 2 hours. Any associated complications will be reported and the time needed to reach the due bladder capacity will be recorded. The procedure of renal transplantation will be carried out according to the hospital protocol and the ureteroneocystostomy will be done by a non-stented Leich Gregoir technique. Assuming that the bladder will regain its activity and full capacity after 8 weeks of transplantation, all patients will be assessed 3 months after transplantation by the following: 1. IPSS questionnaire in order to evaluate the lower urinary tract symptoms. 2. Ascending cystogram. 3. Cystometry. 4. Graft function. Outcome: The primary outcome is to evaluate whether bladder recycling is efficient to restore bladder function prior to renal transplantation in terms of IPSS score, and urodynamic evaluation. The secondary outcome is to evaluate the differences in graft and patients outcome between groups. Power calculation and Statistical analysis: We hypothesized that at 3 months postoperatively; recipients without bladder training will be non-inferior to those underwent bladder training in terms of cystometric capacity. Based on this, to achieve a difference in mean cystometric capacity of 50 cc in favor of bladder training patients, 16 patients in each group are required to achieve a power of 80% and an α error of 0.05. Statistical power is determined using medcalc version 12.5.0.0 software and all statistical analyses will be performed using IBM version 20 statistical software.


Recruitment information / eligibility

Status Recruiting
Enrollment 32
Est. completion date October 2021
Est. primary completion date August 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients maintained on hemodialysis for more than 12 months - have oliguria or anuria - reduced bladder capacity - have no history of lower urinary tract dysfunction and have no evidence of urological cause of renal failure. Exclusion Criteria: - Patients with history of lower urinary tract symptoms before developing renal failure and - those with lower urinary tract disease resulting in renal failure will be excluded

Study Design


Related Conditions & MeSH terms

  • Renal Transplantation Into a Defunctionalized Bladder

Intervention

Behavioral:
bladder recycling
Bladder recycling will be done by the patient after proper education. It will be started by the instillation of the sterile water in the bladder in amount equal to the estimated bladder capacity. Then the amount will be gradually increased till the patient can withstand filling the bladder with 300 cc of sterile water for 2 hours.

Locations

Country Name City State
Egypt Urology and Nephrology Center Al Mansurah El Dakahlia

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary improvement of bladder function after recycling to evaluate whether bladder recycling is efficient to restore bladder function prior to renal transplantation by urodynamic evaluation and ascending cystogram to measure the bladder capacity in cm 3 months
Secondary voiding function after renal transplantation IPSS questionnaire in order to evaluate the lower urinary tract symptoms score ( score range from 0-35)
Ascending cystogram.( capacity in cm, presence of reflux, postvoiding residual urine)
Cystometry ( capacity in cm)
3 months after renal transplantation
Secondary graft function creatinine clearance and estimated GFR by renography ( ml/min/1.73 m2) 1 year