EUCTR2006-003479-11-GB
Active, not recruiting
Not Applicable
The Stroke Oxygen Study. A randomised controlled study of the benefits and risks of routine oxygen treatment after acute stroke - Stroke Oxygen Study
orth Staffordshire Combined Healthcare Trust0 sites6,000 target enrollmentMarch 28, 2007
Drugsoxygen
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- orth Staffordshire Combined Healthcare Trust
- Enrollment
- 6000
- Status
- Active, not recruiting
- Last Updated
- 14 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All adult patients with an acute stroke will be eligible to be considered for study participation. There are no definite guidelines for oxygen treatment after acute stroke, and there is uncertainty amongst stroke physicians about who should be given oxygen and for how long. The eligibility criteria for inclusion into the trial reflect this uncertainty, and allow for randomization of all acute stroke patients who do not have definite indications or definite contraindications for oxygen treatment.
- •Hence adult patients will be eligible for trial inclusion if: They were admitted with symptoms of an acute stroke within the preceding 24 hours, and in the doctor's opinion there is no clear indication for and no clear contraindication against oxygen treatment.
- •The diagnosis of stroke will be made by history and clinical examination and is at the discretion of the admitting doctor. It will based on the WHO criteria (rapidly developing clinical signs of focal or global disturbance of cerebral function, with symptoms lasting 24 hours or longer, or leading to death, with no apparent cause other than of vascular origin). Within the first 24 hours of symptom onset a definite distinction between a stroke and a transient ischaemic attack cannot be made. However, most patients who still have persistent symptoms after one hour will be confirmed to have a stroke. Since waiting for 24 hours for confirmation would unnecessarily delay treatment we omitted the time element from the definition of stroke for the purposes of trial inclusion.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Patients will be excluded from the trial if the responsible doctor considers the patient to have definite indications for or contraindications to oxygen treatment at a rate of 2\-3 L/min. The decision will be left to the responsible clinician. This exclusion criterion has been chosen to ensure that all patients are treated according to best medical practice.
- •Potential indications for oxygen treatment could be: oxygen saturation on air \<90%, hypoxia associated with acute left ventricular failure, severe pneumonia, pulmonary embolus, and chronic respiratory failure patients treated with long term oxygen at home.
- •Potential contraindications to fixed dose oxygen treatment could be type 2 respiratory failure and very severe hypoxia.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
The Stroke Oxygen Pilot Study: a randomised controlled pilot study of the effects of routine oxygen supplementation on functional outcome after acute strokeISRCTN12362720Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)300
Active, not recruiting
Phase 3
PROVE Trial - Positive pRessure therapy in COVid-19 infEctionCTRI/2021/04/033175George Institute for Global Health India
Completed
Phase 1
Randomised trial comparing controlled oxygen therapy with high-flow oxygen therapy in the treatment of patients with Acute Exacerbations of Chronic Obstructive Pulmonary Disease (AECOPD) in the pre-hospital settingChronic Obstructive Pulmonary Disease (COPD)Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD)Respiratory - Chronic obstructive pulmonary diseaseACTRN12609000236291Associate Professor Richard Wood-Baker150
Active, not recruiting
Phase 1
Randomised controlled trial to see if Continuous Positive Airways Pressure will reduce the number of infants transferred from Special Care Nurseries to Intensive care Nurseries.Babies born with respiratory distress in non-tertiary centres.Reproductive Health and Childbirth - Complications of newbornRespiratory - Other respiratory disorders / diseasesACTRN12606000264583Adam Buckmaster300
Completed
Not Applicable
Ambulatory oxygen in interstitial lung diseaseACTRN12617000054314Dr Yet Hong Khor30