Viewing Study NCT06572371



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06572371
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-22

Brief Title: Open Versus Laparoscopic Dismembered Pyeloplasty Among Adult Patients With Primary Pelvi-Ureteric Junction Obstruction
Sponsor: None
Organization: None

Study Overview

Official Title: A Prospective Randomized Study Comparing Open Versus Laparoscopic Dismembered Pyeloplasty Among Adult Patients With Primary Pelvi-Ureteric Junction Obstruction
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To prospectively compare the perioperative morphological and functional outcomes on short and medium term between laparoscopic LP and open pyeloplasty OP patients
Detailed Description: Pelvi-ureteric junction obstruction PUJO is defined as a functionally significant impairment of the flow of urine from the kidneys renal pelvis into the proximal ureter

Open pyeloplasty OP has been the gold standard for PUJO repair since the first successful reconstruction of an obstructed PUJO was accomplished in 1892 and achieves success rates exceeding 90

Various open surgical techniques have been described based on the cause location and length of the PUJO The most popular repair is the Anderson-Hynes dismembered pyeloplasty which has universal application and is accepted as the gold standard of treatment

Now Laparoscopic dismembered pyeloplasty represents a minimally invasive alternative of gold standard open Anderson- Hynes technique that has a comparable successful outcome with open pyeloplasty while avoiding its co-morbidities It is also better than endopylotomy as it deals effectively with the crossing vessel

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None