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Clinical Trial on the Efficacy of Ajwain in the Management of Acute Kidney Injury

Clinical Trial on the Efficacy of Ajwain in the Management of Acute Kidney Injury

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250720066561N1
Enrollment
42
Registered
2025-11-04
Start date
2025-11-06
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Acute Kidney Injury. Acute kidney failure, unspecified

Interventions

Intervention 1: Intervention Group: Participants will receive standard-of-care medical management for AKI plus a daily dose of 2 grams of Ajwain powder. The Ajwain will be administered orally as 500 m

Sponsors

Zabol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: The study population will consist of adult patients, aged 18 to 65 years, admitted to participating hospitals in Zabol, Iran, with a confirmed diagnosis of Acute Kidney Injury (AKI) AKI will be defined and diagnosed according to the Kidney Disease: Improving Global Outcomes (KDIGO) clinical practice guidelines, as meeting any one of the following criteria :An absolute increase in serum creatinine (sCr) of =0.3 mg/dL (=26.5 µmol/L) within 48 hours A relative increase in sCr to =1.5 times the known or presumed baseline value, which is assumed to have occurred within the prior 7 days A documented reduction in urine output to <0.5 mL/kg/hour for a duration of at least 6 consecutive hours.

Exclusion criteria

Exclusion criteria: Pregnancy or current lactation Active malignancy or a history of any malignancy within the past 5 years Severe systemic infection or sepsis at the time of screening Significant hepatic impairment, defined as serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) levels greater than three times the upper limit of the normal reference range Known history of autoimmune disease Current or imminent requirement for renal replacement therapy (RRT) at the time of enrollment, or a history of RRT within the current hospital admission Pre-existing chronic kidney disease (CKD), defined as a known baseline estimated glomerular filtration rate (eGFR) of <60 mL/min/1.73 m². Known hypersensitivity or allergy to Ajwain (Trachyspermum ammi) or any of its constituents

Design outcomes

Primary

MeasureTime frame
Serum Creatinine. Timepoint: Every 72 hours. Method of measurement: Blood Test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAref Shahreki

Zabol University of Medical Sciences

aref.shahreki@gmail.com+98 915 609 0801

Outcome results

None listed

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