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Drug therapy for improving the renal function after kidney transplantation

Investigating the effects of dexmedetomidine infusion during surgery on renal function parameters in patients receiving kidney transplantation

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017101331487N5
Enrollment
50
Registered
2017-10-24
Start date
2017-11-06
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End-stage renal disease. Chronic kidney disease, stage 5

Interventions

Intervention 1: Control. Intervention 2: Dexmedetomidine infusion with dose of 1 mcg/kg/hour.
Placebo
Treatment - Drugs
Control
Dexmedetomidine infusion with dose of 1 mcg/kg/hour

Sponsors

Vice-chancellor for Research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: - end stage renal disease (ESRD) patients - candidate for renal transplant - graft from living donor - age from 18 to 70 years old Exclusion criteria: - bradycardia (HR<50) - hypotension (SBP<100) - ejection fraction below 30% (EF<30%) - transplant from cadaver - simultaneous transplantation of kidney and pancreas - having contraindication for kidney transplantation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Glomerular filtration rate. Timepoint: After patients transfer to ICU, then every one hours until 6 hours after transfer to ICU, then every two hours until 24 hours after ICU and then every 6 hours until the time of discharge. Method of measurement: Biochemistry analyzer.;Creatinine. Timepoint: After patients transfer to ICU, then every one hours until 6 hours after transfer to ICU, then every two hours until 24 hours after ICU and then every 6 hours until the time of discharge. Method of measurement: Biochemistry analyzer.;Urea. Timepoint: After patients transfer to ICU, then every one hours until 6 hours after transfer to ICU, then every two hours until 24 hours after ICU and then every 6 hours until the time of discharge. Method of measurement: Biochemistry analyzer.;Sodium. Timepoint: After patients transfer to ICU, then every one hours until 6 hours after transfer to ICU, then every two hours until 24 hours after ICU and then every 6 hours until the time of discharge. Method of measurement: Biochemistry analyzer.;Hemoglobin. Timepoint: After patients transfer to ICU, then every one hours until 6 hours after transfer to ICU, then every two hours until 24 hours after ICU and then every 6 hours until the time of discharge. Method of measurement: Hematology analyzer.;Hematocrit. Timepoint: After patients transfer to ICU, then every one hours until 6 hours after transfer to ICU, then every two hours until 24 hours after ICU and then every 6 hours until the time of discharge. Method of measurement: Hematology analyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mehrdad Mesbah Kiaee

Iran University of Medical Sciences

dr.mmesbah@gmail.com+98 21 8670 2503

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026