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The effect of intraoperative intravenous mannitol injection on delayed graft function in kidney transplant recipients.

A comparative study of the effect of intravenous mannitol injection during surgery on the rate of delayed transplant performance in kidney transplant recipients in Hashminejad Hospital

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251231068512N1
Enrollment
120
Registered
2026-01-13
Start date
2026-02-20
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Kidney transplant. Kidney transplant failure

Interventions

Intervention 1: Intervention group: the intervention group will receive a 20% Mannitol (D-Mannitol) solution intravenously during surgery. The drug dosage is calculated based on body weight (0.5 mL/kg

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: First-time kidney transplant recipient Age 18–70 years Surgery within the study period Multidisciplinary team approval (Psychiatry, Nephrology, Surgery) Transplant benefits outweigh risks Tolerates surgery and immunosuppression

Exclusion criteria

Exclusion criteria: Underwent renal autotransplantation Known hypersensitivity to mannitol Any adverse reaction that cannot be controlled during the study

Design outcomes

Primary

MeasureTime frame
Delayed Graft Function. Timepoint: 10 days post-transplant. Method of measurement: Clinical examination.

Secondary

MeasureTime frame
Serum creatinine level. Timepoint: Up to 10 days after transplantation. Method of measurement: Test.;24-hour urine volume. Timepoint: 24 hours after receiving the transplant. Method of measurement: Test.;Deaths. Timepoint: Up to 3 months after transplantation. Method of measurement: Follow-up.;Cold ischemic time. Timepoint: During the transplant operation. Method of measurement: observation.;Warm Ischemic Time. Timepoint: During the transplant operation. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaber Khoramabadi

Iran University of Medical Sciences

Drsaberkhorramabadi@gmail.com+98 21 81161

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026