MedPath

Targeted OXYgen Therapy in Critical Illness

Not Applicable
Completed
Conditions
Critical Illness
Respiratory Failure
Interventions
Registration Number
NCT03287466
Lead Sponsor
University College, London
Brief Summary

The investigators propose to conduct a feasibility, multi-centre, randomised controlled trial of targeted oxygen therapy in adult critically ill patients receiving mechanical ventilation via an endotracheal tube as part of their treatment for respiratory failure. Participants will be allocated to either a normal blood oxygen target group or a lower than normal blood oxygen target group. The primary purpose of the study will be to assess the feasibility of recruiting complex patients who lack capacity into a clinical trial in which oxygenation is being assessed, and that the clinicians responsible for these patients are able to deliver the intervention effectively. The safety of using a lower than normal blood oxygen target will also be assessed and blood samples taken for subsequent investigation of the biological mechanisms underlying the observed changes.

Participants will be randomised (1:1) into either an intervention or control group. The intervention in this trial is tightly controlled administration of oxygen to patients to achieve a haemoglobin oxygen saturation (SpO2) of 88-92%. The control group will also have tightly controlled oxygen administration, but to achieve an SpO2 of 96% or above. The target for the control group represents a normal SpO2, whilst that in the intervention group is lower than what is considered to be normal. It should be noted that although lower than normal, this SpO2 is close to what the general public experience when travelling by pressurised aircraft as the fractional inspired oxygen concentration in that situation is only 0.15-0.17 (15-17%).

The controlled oxygen administration would commence as soon as possible after admission to the critical care unit and end following removal of the participant's artificial breathing tube. The researchers and clinical team cannot be blinded to treatment allocation, due to the nature of the intervention. Those analysing the data will be blinded to the intervention.

Detailed Description

The investigators aim is to determine whether revising standard targets for blood oxygen levels in patients requiring artificial ventilation on a critical care unit is feasible and whether this affects specific blood biomarker levels.

Investigators in this area of expertise currently lack the information necessary to determine how much oxygen should be given to adult critically ill patients on a mechanical ventilator to assist their breathing in order to achieve the best clinical outcomes i.e. minimal morbidity and mortality. Excessive oxygen administration (both its concentration and duration) and hyperoxaemia (an excessively high blood oxygen level) are known to be harmful to critically ill patients. The reason for this is that oxygen in high concentration is toxic, because it results in the release of molecules called reactive oxygen species (ROS). ROS lead to a state known as 'oxidative stress', in which cells and tissues are rapidly destroyed by these destructive molecules.

The difficulty with treating critically ill patients is that they are usually extremely unwell, requiring artificial ventilation to support their breathing. Unfortunately, these patients appear to be exceptionally prone to the harms of oxidative stress, leading to permanent damage of their lungs. Yet it is precisely this group of patients who require high concentration oxygen to keep their blood oxygen levels within the normal. It has therefore been hypothesised that using lower blood oxygen targets than usual may be beneficial to these patients through the avoidance of excessively high concentrations of oxygen. The investigator proposes that in mechanically ventilated critically ill patients harm (morbidity and mortality) will be reduced by using 'targeted oxygen therapy' (TO2T) to achieve lower blood oxygen levels than normal when compared to standard practice (normal blood oxygen levels). The levels are only moderately lower than normal and well within what most clinicians would consider to be safe in these patients.

Prior to any large-scale study, it is important to understand if this approach to managing critically ill patients is feasible. This prospective, dual site randomised controlled trial will therefore establish whether it is possible to conduct a trial in which blood oxygen levels are carefully titrated by the critical care team, to achieve specific targets. Participants will be allocated into one of two groups: i) normal blood oxygen levels, and ii) low blood oxygen levels. For the time that participants are artificially ventilated by a breathing (endotracheal) tube, they will remain in their allocated treatment group. Information will be collected from the patient's charts and records during their stay on the CCU to assess the impact of the treatment. A series of blood samples will also be collected from participants to quantify the degree of oxidative stress through the measurement of several specific biomarkers. A total of 60 patients will be enrolled at two sites.

As oxygen is a drug that is administered to almost every patient admitted to a critical care unit (CCU), it is imperative that decisions regarding oxygenation are based upon evidence rather than conjecture. Limited work has been undertaken to date to understand whether lowering blood oxygen levels is achievable in this complex patient group. The information from this study will be used to design a subsequent much larger study to fully evaluate whether TO2T to achieve lower blood oxygen levels saves lives in critically ill patients. If lower blood oxygen levels improve survival in critically ill patients implementation of this intervention could have an immediate and cost-effective impact across the entire National Health Service.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
34
Inclusion Criteria
  • Unplanned admission to a critical care unit
  • 18 years of age and above (no upper age limit)
  • Respiratory failure forms part of the admission diagnosis
  • The patient is mechanically ventilated via an endotracheal tube
  • The patient is expected to receive mechanical ventilation for > 24 hours
Exclusion Criteria
  • Admission following surgery (elective or unplanned)

  • Those patients expected to die within 24 hours of admission to ICU *

  • Pregnant females

  • Admission post-cardiac arrest

  • Admission post trauma (including traumatic brain injury)

  • Known sickle cell trait or disease

  • Ongoing significant haemorrhage or profound anaemia

  • Severe peripheral vascular disease

  • Severe pulmonary hypertension

  • Other medical conditions where mild hypoxaemia would be contra-indicated ***

  • Patients participating in other interventional clinical trials

    • As determined by the responsible clinical team ** As determined by the responsible clinical team and /or research team

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SpO2 88-92%OxygenThe intervention is targeted oxygen therapy (TO2T) to achieve an arterial haemoglobin oxygen saturation (SpO2) of 88-92%.
Current best practiceOxygenThe control group will have no specific SpO2 targets. Clinicians will be able to target SpO2 according to parameters they feel are suitable for the patient, according to standard UK practice.
Primary Outcome Measures
NameTimeMethod
Feasibility to recruit15 Months

Ability to recruit

Secondary Outcome Measures
NameTimeMethod
Measurement of blood pressureup to 21 days

Measurement of blood pressure

Measurement of vasopressor dosesup to 21 days

Measurement of vasopressor doses

Measurement of inotrope dosesup to 21 days

Measurement of inotrope doses

Adverse events90 days

Adverse events

Measurement of arterial blood gasesup to 21 days

Measurement of arterial blood gases

Time to extubation / detachment from mechanical ventilationup to 21 days

Time to extubation / detachment from mechanical ventilation

Measurement of vasopressor free days on ICUup to 21 days

Measurement of vasopressor free days on ICU

The need for renal replacement therapyup to 21 days

The need for renal replacement therapy

Measurement of fraction of inspired oxygenup to 21 days

Measurement of fraction of inspired oxygen

Measurement of cardiac output and stroke volume (if measured)up to 21 days

Measurement of cardiac output and stroke volume (if measured)

Measurement of bilirubinup to 21 days

Measurement of bilirubin

Mortality rates90 days

Days alive

Days alive out of Hospital90 days

Days alive out of Hospital

Mechanical ventilation free days on ICUup to 21 days

Mechanical ventilation free days on ICU

Measurement of oxygen saturationup to 21 days

Measurement of oxygen saturation

Measurement of daily fluid balanceup to 21 days

Measurement of daily fluid balance

Measurement of inotrope free days on ICUup to 21 days

Measurement of inotrope free days on ICU

Measurement of heart rateup to 21 days

Measurement of heart rate

Measurement of cardiac rhythmup to 21 days

Measurement of cardiac rhythm

Measurement of Ureaup to 21 days

Measurement of Urea

Measurement of creatinineup to 21 days

Measurement of creatinine

Measurement of urine outputup to 21 days

Measurement of urine output

Measurement of transaminasesup to 21 days

Measurement of transaminases

Renal replacement therapy free days on ICUup to 21 days

Renal replacement therapy free days on ICU

Measurement of blood clotting valuesup to 21 days

Measurement of blood clotting values

Measurement of blood lactateup to 21 days

Measurement of blood lactate

Measurement of Troponinup to 21 days

Measurement of Troponin

APACHE II score changeup to 21 days

Acute Physiology and Chronic Health Evaluation (APACHE) II score change

SOFA score changeup to 21 days

Sequential Organ Failure Assessment (SOFA) score change

Length of ICU stayup to 21 days

Length of stay in intensive care unit

Length of hospital stay90 days

Length of hospital stay

Trial Locations

Locations (1)

Royal Free Hospital

🇬🇧

London, United Kingdom

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