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Ubiquinol (Reduced COQ10) for Patients With Sepsis

Ubiquinol (Reduced COQ10) for Patients With Sepsis

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01948063
Enrollment
38
Registered
2013-09-23
Start date
2012-10-31
Completion date
2014-04-30
Last updated
2017-04-24

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

Conditions

Sepsis

Brief summary

This study aims to determine if Ubiquinol (reduced form of COQ10) will attenuate mitochondrial injury and decrease inflammatory response in patients suffering from sepsis.

Detailed description

Severe sepsis and septic shock are the cause of significant morbidity and mortality worldwide. An estimated 751,000 (3 per 1,000 population) cases of severe sepsis occur in the United States each year, resulting in approximately 215,000 deaths. Septic shock is characterized by hypotension, hypermetabolic state, lactic acidosis, and potentially death. In addition, the economic burden on the health care system for patients suffering from severe sepsis is striking. Weycker et al. report that patients suffering from severe sepsis will require an average of $45,000 dollars of medical care cost on their index admission and up to $78,500 dollars in the first year post-diagnosis. These figures rival such entities as acute myocardial infarction, trauma, and stroke. Whereas a significant amount of research and therapeutic interventions have been focused on the early hours of diseases such as acute myocardial infarction, stroke, and trauma, less attention has been given to the initial stages of severe sepsis and septic shock. Coenzyme Q10 (CoQ10) is a safe and feasible medicinal intervention with a strong scientific rationale for use in septic shock. CoQ10 is a key component of the mitochondria, serving as an electron transport medium between complex I/II and complex III. A lesion at this point in the electron transport chain results in an inadequate production of ATP (adenosine triphosphate) for the cell. In septic shock, CoQ10 levels are profoundly decreased and therefore production of energy may be compromised. CoQ10 has two essential roles in critically ill patients with sepsis: 1) production of ATP and 2) reduction of free oxygen radicals. CoQ10's key role in the electron transport chain may prevent the well-described mitochondrial dysfunction that occurs in patients with septic shock. Thus, these two essential roles form the pathophysiological basis for this proposed study. In the following proposal, the investigators plan to perform a pilot study to evaluate the capacity for ubiquinol (reduced form of COQ10) to attenuate mitochondrial injury, to attenuate inflammation/vascular endothelial injury, the effect on the human metabolome, and to be absorbed. The overall goal of this line of research will be to determine if CoQ10 will attenuate oxidative injury and improve mitochondrial function leading to overall improved outcome in patients suffering from septic shock. In order to achieve this long-term goal, the investigators propose this pilot and feasibility trial to determine CoQ10 absorption in critical illness, capacity to mitigate inflammatory injury and oxidative injury, and ability to maintain mitochondrial electron transport chain functionality. This pilot study will also provide key feasibility data on blinding and other logistical issues necessary for execution of a larger-scale investigation.

Interventions

Depending on the patient's ability to swallow pills, patients in the experimental group will receive 200mg Ubiquinol in either a pill or a liquid. The liquid form of the study med will be mixed with 50 milliliters of Ensure (a dietary supplement) to ensure blinding. This will be given every 12 hours for 7 days or until hospital discharge.

DIETARY_SUPPLEMENTPlacebo

Depending on the patient's ability to swallow pills, patients in the control group will receive a placebo pill or a liquid placebo, which is 50 milliliters of Ensure (a dietary supplement). This will be given every 12 hours for 7 days or until hospital discharge.

Sponsors

Kaneka Medical America LLC
CollaboratorINDUSTRY
Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Over 18 years old * Suspected or confirmed infection * Presence of 2 or more systemic inflammatory response syndrome (SIRS) criteria * Admission to the ICU

Exclusion criteria

* Under 18 years old * Current CoQ10 supplementation * Unable to receive enteral medications * Would need a nasogastric or orogastric tube solely for the purposes of the study * Pregnancy, incarceration, mentally disability * Patient confirmed Comfort measures only, Do not resuscitate (DNR) and/or Do not intubate. Patients with DNR but intubated and being provided full care are eligible

Design outcomes

Primary

MeasureTime frameDescription
CoQ10 Levels24 hours after study drug administrationTotal CoQ10 levels (mcg/mL) at 24 hours post study drug admission.

Countries

United States

Participant flow

Pre-assignment details

1 patient was randomized in the placebo group but the blood was accidentally thawed why this patient was excluded. 2 patients were randomized in the Ubiquinol group but never received the treatment (one because of an exclusion criteria and one because of a Boston-wide mass casualty event). These were also excluded.

Participants by arm

ArmCount
Placebo
Patients will receive a placebo pill or a liquid placebo. The liquid placebo is 50 milliliters of Ensure (a dietary supplement). Placebo will be given every 12 hours for 7 days or until hospital discharge.
19
Ubiquinol
Patients will receive 200mg of Ubiquinol in either a pill or a liquid. The liquid form of the study med will be mixed with 50 milliliters of Ensure (a dietary supplement) to ensure blinding. This will be given every 12 hours for 7 days or until hospital discharge.
19
Total38

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyBlood samples were accidentally thawed10
Overall StudyBoston MCI halted research protocol01
Overall StudyDiscovered an enrollment in other study01

Baseline characteristics

CharacteristicPlaceboTotalUbiquinol
Age, Continuous64 Years
STANDARD_DEVIATION 14
62 Years
STANDARD_DEVIATION 15
60 Years
STANDARD_DEVIATION 18
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants1 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
15 Participants33 Participants18 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
3 Participants4 Participants1 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
1 Participants1 Participants0 Participants
Race (NIH/OMB)
Black or African American
4 Participants7 Participants3 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
1 Participants1 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants2 Participants2 Participants
Race (NIH/OMB)
White
13 Participants27 Participants14 Participants
Region of Enrollment
United States
19 participants38 participants19 participants
Sex: Female, Male
Female
11 Participants18 Participants7 Participants
Sex: Female, Male
Male
8 Participants20 Participants12 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
4 / 192 / 19
other
Total, other adverse events
1 / 190 / 19
serious
Total, serious adverse events
0 / 190 / 19

Outcome results

Primary

CoQ10 Levels

Total CoQ10 levels (mcg/mL) at 24 hours post study drug admission.

Time frame: 24 hours after study drug administration

ArmMeasureValue (MEDIAN)
PlaceboCoQ10 Levels0.38 (mcg/mL)
UbiquinolCoQ10 Levels0.87 (mcg/mL)

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026