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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05035303
Other study ID # RC-200310
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 10, 2020
Est. completion date January 1, 2022

Study information

Verified date January 2022
Source Benha University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

during PCNL; A few milliliters of nor-epinephrine is injected into the intended tract after puncture of pelvicalyceal system and before its dilatation compared to injection of saline (placebo). hemoglobin change & blood loss is estimated and will compared.


Description:

All patients of are positioned in lithotomy position and 6 F open tip ureteral catheter is fixed by cystoscope. Then, A pelvicalyceal system is punctured under ultrasound and/or fluoroscopic guidance, then a 18 Gauge (G) puncture needle is introduced toward the desired calyx and a 0.038 inch guide wire is inserted. then 20 G Chiba needle is introduced alongside the puncture needle for infiltration of the whole tract by either a few milliliters of nor-epinephrine or saline. then, the tract is dilated over the guide wire, lastly an Amplatz sheath was inserted. nephroscope is used for stones disintegration by pneumatic or laser lithotripter . Fragments are washed out or removed by forceps.


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date January 1, 2022
Est. primary completion date November 10, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - renal stones>2 cm Exclusion Criteria: - coagulopathy, congenital anomalies, active Urinary tract infections

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Nor-Epinephrine injection versus saline during PCNL
The PCNL tract is infiltrated by Nor-Epinephrine or Normal Saline before its dilatation.

Locations

Country Name City State
Egypt Banha university hospital Banha Qalubia
Egypt Banha University Hospitals Banha Kalubiaya

Sponsors (1)

Lead Sponsor Collaborator
Benha University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary hemoglobin drop the lower drop is better 72 hours post intervention
Primary blood loss the lower loss is better immediately after surgery
Secondary stone free rate the higher is better within 3 months post-operative
Secondary adverse events the lower is better within 30 days post-operative
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