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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03695991
Other study ID # PCNHK
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 2019
Est. completion date December 2020

Study information

Verified date April 2019
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hydronephrosis describes a condition of urine-filled dilation of the collecting system. Normally, urine flows through the urinary tract with minimal or low pressure. If the build-up of excess fluid in the urinary collecting system continues, there will be an increase in pressure and atrophy of renal cortex. If hydronephrosis is left untreated for a long time, renal damage with permanent loss of function occurs


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 62
Est. completion date December 2020
Est. primary completion date October 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- 1) Patients for whom a percutaneous nephrostomy is indicated provided that the hydronephrosis is advanced ( parenchymal thickness not more than 5 mm ) 2) Patients for whom a nephrectomy is planned for a seemingly poorly functioning kidney along with either

Exclusion Criteria:

1. Target kidney is the only functioning or better functioning kidney or otherwise substantially contributing to the total renal function, so nephrectomy is not likely.

2. Emergency cases where the general condition of the patient cannot withstand the logistics of undergoing a radioisotope study eg

3. Malignancy in the target kidney

4. Patients unlikely to undergo a nephrectomy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
percutaneous nephrostomy
The percutaneous nephrostomy will be done under sonographic or fluoroscopic guidance. Establishment of intravenous access and antibiotics will be performed half an hour prior to procedure particularly in patients presenting with urinary tract infection. The procedure will be done under local anesthesia but general anesthesia may be used for uncooperative patients. percutaneous nephrostomy will be performed in the prone position, however, in case of relative contraindication to prone position

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary The rate of increase in glomerular filtration rate after intervention the radioisotope measurement of glomerular filtration rate will be done before and after insertion of percutaneous nephrostomy tube 3 weeks
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