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| Study Type: | Interventional |
|---|---|
| Study Design: | Allocation: Randomized; Endpoint Classification: Safety/Efficacy Study; Intervention Model: Parallel Assignment; Masking: Double Blind (Subject, Caregiver, Outcomes Assessor); Primary Purpose: Treatment |
| Condition: |
Ischemic Stroke |
| Interventions: |
Drug: NBO (Normobaric Oxygen) Drug: Room Air |
Participant Flow
| Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations |
|---|
| February 2007-June 2009 |
| Significant events and approaches for the overall study following participant enrollment, but prior to group assignment |
|---|
| No text entered. |
| Description | |
|---|---|
| Normobaric Oxygen | Oxygen, inhaled at 30-45L/min via a facemask for 8 hours |
| Room Air | Room Air, inhaled at 30-45L/min via a facemask for 8 hours |
| Normobaric Oxygen | Room Air | |
|---|---|---|
| STARTED | 43 | 42 |
| COMPLETED | 43 | 41 |
| NOT COMPLETED | 0 | 1 |
| Withdrawal by Subject | 0 | 1 |
Baseline Characteristics
| Description | |
|---|---|
| Normobaric Oxygen | Oxygen, inhaled at 30-45L/min via a facemask for 8 hours |
| Room Air | Room Air, inhaled at 30-45L/min via a facemask for 8 hours |
| Normobaric Oxygen | Room Air | Total | |
|---|---|---|---|
|
Number of Participants
[units: participants] |
43 | 42 | 85 |
|
Age
[units: years] Mean ± Standard Deviation |
74.1 ± 14 | 73.4 ± 14 | 73.7 ± 14 |
|
Gender
[units: participants] |
|||
| Female | 27 | 17 | 44 |
| Male | 16 | 25 | 41 |
|
Ethnicity (NIH/OMB)
[units: participants] |
|||
| Hispanic or Latino | 0 | 6 | 6 |
| Not Hispanic or Latino | 42 | 36 | 78 |
| Unknown or Not Reported | 1 | 0 | 1 |
|
Race (NIH/OMB)
[units: participants] |
|||
| American Indian or Alaska Native | 0 | 0 | 0 |
| Asian | 1 | 2 | 3 |
| Native Hawaiian or Other Pacific Islander | 0 | 0 | 0 |
| Black or African American | 2 | 1 | 3 |
| White | 40 | 39 | 79 |
| More than one race | 0 | 0 | 0 |
| Unknown or Not Reported | 0 | 0 | 0 |
Outcome Measures
| 1. Primary: | Primary Safety Outcome Measure is a Comparison of the Change in National Institutes of Health Stroke Scale (NIHSS) Scores From Baseline to 24 Hours (After Therapy) in the Two Groups. [ Time Frame: 24 hours ] |
| 2. Primary: | Primary Efficacy Outcome Measure is a Comparison of the Change in National Institutes of Health Stroke Scale (NIHSS) Scores From Baseline to 4 Hours (During Therapy) in the Two Groups. [ Time Frame: 4 hours after starting treatment ] |
More Information
| Principal Investigators are NOT employed by the organization sponsoring the study. |
| There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed. |
| Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data |
|---|
| THESE ARE *PRELIMINARY* RESULTS. |
| Responsible Party: | Aneesh B. Singhal, MD, Massachusetts General Hospital |
| ClinicalTrials.gov Identifier: | NCT00414726 History of Changes |
| Other Study ID Numbers: | R01NS051412, P50NS051343 |
| Study First Received: | December 21, 2006 |
| Results First Received: | July 1, 2010 |
| Last Updated: | October 28, 2011 |
| Health Authority: | United States: Food and Drug Administration |