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Evaluation of cranberry juice on bacteriuria and puria in spinal cord lesion.

Evaluation of cranberry juice on bacteriuria and puria in spinal cord lesion.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201112073912N4
Enrollment
60
Registered
2012-06-18
Start date
2012-12-01
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

Spinal Cord Lesion. Injury of spinal cord, level unspecified

Interventions

Intervention 1: Case: 250cc cranberry juice placebo daily with meals for 2 weeks. Intervention 2: Control : 250cc placebo daily with meals for 2 weeks.
Prevention
Case: 250cc cranberry juice placebo daily with meals for 2 weeks.
Control : 250cc placebo daily with meals for 2 weeks.

Sponsors

Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 60 Years

Inclusion criteria

Inclusion criteria: Exclusion criteria: Patients with definite indications for antibiotic treatment (pyocystitis, symptomatic UTI, fever, flank tenderness);Patients with creatinine levels greater than 1.5 gr/dl;Patients with gastrointestinal intolerance or those with allergy to cranberries;Patients who did not complete the clinical trial. inclusion criteria:patients with spinal cord injery , age between 19-60 y;patients (51 male and 9 female) with creatinine levels below 1.5 mg/dl and in the analysis of their urine white blood cell (WBC) counts were greater than 10 in a high-powered field (pyuria) or with a presence of bacteriuria (>= 104 cc/ml) in their urine culture

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Colony count. Timepoint: Before and 2 weeks after ntervention. Method of measurement: paraclinic.

Secondary

MeasureTime frame
Odor of urine. Timepoint: before and 2weeks after intervention. Method of measurement: paraclinic.;PH OF urine. Timepoint: before and 2weeks after intervention. Method of measurement: paraclinic.;Type of microorganism. Timepoint: before and 2weeks after intervention. Method of measurement: paraclinic.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKobra Noorian

Shahrekord University of Medical Sciences

noorian@skums.ac.ir+98 38 1333 5648

Outcome results

None listed

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