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The effectiveness of infusion of ascorbic acid and thiamine on the clinical implications of severe sepsis patients admitted to ICU

The effectiveness and non effectiveness of infusion of high-dose ascorbic acid and thiamine as an auxiliary treatment on the clinical implications of severe sepsis patients admitted to ICU

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130812014333N78
Enrollment
30
Registered
2017-12-03
Start date
2017-12-06
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

Sepsis. Sepsis, unspecified

Interventions

Intervention 1: The intervention group will receive 50 mg intravenous ascorbic every 6 hours and up to 6 grams and 200 mg thiamine every 12 hours for 4 days. Intervention 2: The control group will rec
Treatment - Drugs
Placebo
The intervention group will receive 50 mg intravenous ascorbic every 6 hours and up to 6 grams and 200 mg thiamine every 12 hours for 4 days.
The control group will receive 50 mg of placebo for 4 days.

Sponsors

Vice chancellor for research of Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Dysfunction of organs and SOFA score = 2 in patients whose antibiotic therapy is diagnosed. SOFA score = 2 in patients whose antibiotic therapy is diagnosed.

Exclusion criteria

Exclusion criteria: Pregnant women and people under the age of 18; ; Allergy to ascorbic acid, Chronic hemodialysis, Hemochromatotomy Sickness to G6PD Nephropathy oxalate or bilateral erlithiasis Receive simultaneously other antioxidants Patients with acquired immunodeficiency disease

Design outcomes

Primary

MeasureTime frame
Organ dysfunction. Timepoint: The first day and fourth day study. Method of measurement: Based on laboratory and clinical criteria.;Length of stay in ICU. Timepoint: 28 days after intervention. Method of measurement: Based on patient records.;Mortality rate. Timepoint: 28 days after intervention. Method of measurement: Based on patient records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Bahrami

Kermanshah University of Medical Sciences

alirezab8188@gmail.Com+98 83 3427 6301

Outcome results

None listed

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