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Assessment of Anti-inflammatory effect of Azithromycin on kidney donor and potential effect on recipient

Assessment of Anti-inflammatory effect of Azithromycin on kidney donor and potential effect on recipient

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201606141853N11
Enrollment
36
Registered
2016-09-05
Start date
2016-06-21
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

Transplanted kidney function. Chronic kidney disease, stage 5

Interventions

Intervention 1: Intervention group: Capsule of Azithromycin 1 g, 24 hours before nephrectomy, Made in Iran. Intervention 2: Control group: Capsule of placebo 1 g, 24 hours before nephrectomy, Made in
Treatment - Drugs
Placebo
Intervention group: Capsule of Azithromycin 1 g, 24 hours before nephrectomy, Made in Iran
Control group: Capsule of placebo 1 g, 24 hours before nephrectomy, Made in Iran

Sponsors

Urology Research Centre, Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Alive or cadaveric donor; Sign the inform consent by donor or Family of cadaver Exclusion criteria: Allergic components or allergic to various brands of Azithromycin; Severe medical disease like heart, liver, renal, hematological; respiratory, cardiovascular, psychiatric or other problem pre transplantation in donor; Consumption of other medication including Macrolides family; Involvement in additional clinical trials at the same time

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
GFR. Timepoint: 1 day, 2 days, 4 days, 30 days and 90 days after transplantation. Method of measurement: Cockcroft-Gault Equation.

Secondary

MeasureTime frame
Complication. Timepoint: 1 day, 2 days, 4 days, 30 days and 90 days after transplantation. Method of measurement: Registration of physical examination, medical history and paraclinical findings.;Pain score in donors. Timepoint: 1 day, 2 days and 4 days after transplantation. Method of measurement: Visual Analog Scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mojtaba Teimoori

Urology Research Center

urc1384@yahoo.com;mojtaba_teimoori@yahoo.com+98 13 3352 5259

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 6, 2026