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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03107858
Other study ID # NorepivsDopamine
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received March 24, 2017
Last updated October 18, 2017
Start date November 1, 2017
Est. completion date November 1, 2019

Study information

Verified date October 2017
Source Assiut University
Contact Ahmed Elkadi, MBBC
Phone +201007485190
Email ahmedkader333@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Renal transplantation is now recognized as a treatment of choice for patients with chronic renal failure with end-stage renal disease. Renal transplantations are associated with better quality of life, better cost/benefit ratio, and possibly longer survival. Significant changes in blood pressure are common throughout the surgical procedure for kidney transplantation. All efforts are made to maintain an appropriate level of blood pressure by using an adequate intravascular volume and vasopressor administration. All efforts are made to maintain an appropriate level of blood pressure by using an adequate intravascular volume and vasopressor administration. All efforts are made to maintain an appropriate level of blood pressure by using an adequate intravascular volume and vasopressor administration. All efforts are made to maintain an appropriate level of blood pressure by using an adequate intravascular volume and vasopressor administration.


Recruitment information / eligibility

Status Recruiting
Enrollment 44
Est. completion date November 1, 2019
Est. primary completion date January 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients scheduled for a living donor kidney transplantation

Exclusion Criteria:

- Patients (less than 18 years old)

- Patients' refusal of consenting for enrolment in the study

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Norepinephrine
Norepinephrine infusion will be used at a starting dose of 0.05µg/kg/min. Dose range: 0.05 -0.15 µg/kg/min. Infusion will be started with arterial decamping and continues till 24 hours postoperative
Dopamine
Dopamine infusion will be used at a starting dose of 5µg/kg/min. Dose range: 5 -15 µg/kg/min. Infusion will be started with arterial decamping and continues till 24 hours postoperative

Locations

Country Name City State
Egypt Assiut University Hospital Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary serum creatinine postoperative four hours postoperatively
Secondary blood urea postoperative four hours postoperatively
Secondary urine output postoperative over 24 hours
Secondary renal artery diameter Measured postoperative through renal artery Doppler four hours postoperatively
Secondary renal artery blood flow Measured postoperative through renal artery Doppler four hours postoperatively
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