Skip to content

Clinical Trial of Antioxidant Therapy in Patients With Septic Shock

Randomized Controlled Clinical Trial of Antioxidant Therapy in Critically Ill Patients With Septic Shock: Analysis Before and After Treatment of the Oxidative Stress

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03557229
Enrollment
131
Registered
2018-06-14
Start date
2018-07-23
Completion date
2022-06-30
Last updated
2021-08-10

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

Conditions

Oxidative Stress, Septic Shock

Keywords

Oxidative Stress, Sepsis, Treatment, Antioxidant therapy

Brief summary

Sepsis and septic shock are public health problems worldwide that represents an excessive cost for health systems. Despite the great technological and research advances, mortality can reach up to 80% in patients with multiple organ failure (FOM). Therapeutic studies focused on evaluating the usefulness of the use of antioxidants have shown different outcomes and results. This randomized clinical trial in patients with septic shock at two general intensive care units try to evaluate the usefulness of four different antioxidant therapies added to the conventional treatment, which includes: n-acetyl cysteine, vitamin C, vitamin E and melatonin. Measurement of parameters before and after treatment of oxidative stress includes nitrates and nitrites, lipid peroxidation, glutathione peroxidase, glutathione s transferase, extracellular activity of SOD, GSH concentration and evaluation of total antioxidant capacity. The investigators will also evaluate the clinical impact of antioxidant therapy with the SOFA score.

Interventions

Oral: 50 mg once daily for 5 days

DRUGVitamin C 1 GM Oral Tablet

Oral: 1 GM every 6 hours for 5 days

Oral: 400 UNT every 8 hours for 5 days

DRUGN-acetylcysteine

Oral: 1200 mg every 12 hours for 5 days

Sponsors

American British Cowdray Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of septic shock in the last 24 hours characterized by refractory hypotension and vasopressor requirement despite sufficient fluid resuscitation (20 mL/kg of colloids or 40 mL/kg of crystalloids) to maintain a blood pressure ≥ 65 mmHg with a lactate\> 2 mmol/L. * Admitted to the ICU of the ABC Medical Center. * Give informed consent.

Exclusion criteria

* Patients who refuse to be included. * Chronic or recent use of steroids. * Use of statins. * Patients receiving some type of antioxidant treatment. * Any contraindication to the use of vitamin C, vitamin E, n-acetylcysteine or melatonin. * Pregnant women.

Design outcomes

Primary

MeasureTime frameDescription
Organic failure measurement by the Sequential Organ Failure Assessment Score (SOFA)Up to 7 days (1 week). From date of randomization and every 24 hours until discharge from the intensive care unit or date of death from any cause, whichever came first, assessed up to 7 days.The SOFA score is used to track a person's status during the stay in an intensive care unit (ICU) to determine the extent of a person's organ function or rate of failure. The score is based on six different scores, one each for the respiratory, cardiovascular, hepatic, coagulation, renal and neurological systems. Each organ system is assigned a point value from 0 (normal) to 4 (high degree of dysfunction/failure). The worst physiological variables is collected serially every 24 hours of a patient's ICU admission. The worst measurement is defined as the measure that correlated to the highest number of points. The SOFA score ranges from 0 to 24. The investigators are going to evaluate the daily total score and the trend before and after the administration of the therapy.

Secondary

MeasureTime frameDescription
Glutathione Peroxidase Enzyme ActivityImmediately before treatment and 48 hours after therapyAntioxidant status
Glutathione concentrationImmediately before treatment and 48 hours after therapyAntioxidant status
SeleniumImmediately before treatment and 48 hours after therapyAntioxidant status
Vitamin CImmediately before treatment and 48 hours after therapyAntioxidant status
ThioredoxinImmediately before treatment and 48 hours after therapyAntioxidant status
CarbonylationImmediately before treatment and 48 hours after therapyPro-oxidant status
Nitrates and nitrites levelsImmediately before treatment and 48 hours after therapyOxidative stress
Malondialdehyde levelsImmediately before treatment and 48 hours after therapyLipid peroxidation
Total antioxidant capacityImmediately before treatment and 48 hours after therapyAntioxidant status
Glutathione S-transferase ActivityImmediately before treatment and 48 hours after therapyAntioxidant status
Extracellular Superoxide Dismutase ActivityImmediately before treatment and 48 hours after therapyAntioxidant status

Other

MeasureTime frameDescription
IL-6Immediately before treatment and 48 hours after therapyInflammatory Response Pathway
Ionized Ca2+Immediately before treatment and 48 hours after therapyElectrolytes
Ionized Mg2+Immediately before treatment and 48 hours after therapyElectrolytes
IL-1Immediately before treatment and 48 hours after therapyInflammatory Response Pathway
TNF-αImmediately before treatment and 48 hours after therapyInflammatory Response Pathway

Countries

Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026