Efficacy and Safety Trial of Transcranial Laser Therapy Within 24 Hours From Stroke Onset (NEST-3)
Status: | Recruiting |
---|---|
Conditions: | Peripheral Vascular Disease, Neurology |
Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology |
Healthy: | No |
Age Range: | Any |
Updated: | 10/21/2012 |
Start Date: | September 2010 |
Contact: | Steven P Richieri |
Email: | srichieri@photothera.com |
Phone: | 760-692-4924 |
NeuroThera® Efficacy and Safety Trial - 3 (NEST-3) A Double-blind, Randomized, Sham-controlled, Parallel Group, Multicenter, Pivotal Study to Assess the Safety and Efficacy of Transcranial Laser Therapy With the NeuroThera® Laser System for the Treatment of Acute Ischemic Stroke Within 24 Hours of Stroke Onset
The purpose of this pivotal study is to demonstrate safety and efficacy of transcranial
laser therapy (TLT) with the NeuroThera® Laser System in the treatment of subjects diagnosed
with acute ischemic stroke. The initiation of the TLT procedure must be feasible for each
subject between 4.5 and 24 hours of stroke onset.
Inclusion Criteria:
1. Clinical diagnosis of acute ischemic stroke
2. Subject is not a candidate for treatment with neurothrombectomy
3. Initiation of the TLT procedure begins between 4.5 and 24 hours
4. Baseline NIHSS score range: 7-17
5. Full functional independence just prior to the present stroke episode
6. Negative pregnancy test in females of childbearing potential
7. Subject Informed Consent obtained prior to enrollment into this study
Exclusion Criteria:
1. Evidence of an intracranial, subdural, or subarachnoid hemorrhage
2. Acute ischemic strokes located exclusively in the brainstem, or cerebellum, or small
deep infarctions, or massive hemispheric strokes
3. Seizure at stroke onset or within the 7 days prior to stroke onset
4. Sustained blood glucose >300 or <60 mg/dl
5. Sustained hypertension (SBP >220 mmHg or DBP >140 mmHg)
6. Sustained hypotension (SBP <80 mmHg or DBP <50 mmHg)
7. A presumed and/or confirmed septic embolus
8. History of CNS vascular disease (e.g. aneurysm, AVM) or history of CNS disease or
damage (e.g. neoplasm or dementia) which may influence the subject's outcome
assessment.
9. Head implant of any kind
10. Significant skin condition of the scalp (eg. psoriasis)
11. Use of any intravenous or intra-arterial thrombolytic medication
12. Use of any diagnostic or therapeutic interventional neurovascular procedure
13. Female who is pregnant or lactating or who is of childbearing potential and not using
a medically acceptable method of birth control.
We found this trial at
25
sites
3181 S.W. Sam Jackson Park Rd.
Portland, Oregon 97201
Portland, Oregon 97201
503 494-8311
Oregon Health Sciences University In 1887, the inaugural class of the University of Oregon Medical...
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Houston Methodist Hospital Houston Methodist is comprised of a leading academic medical center in the...
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Sentara Norfolk General Hospital Sentara Norfolk General Hospital is recognized as the number one ranked...
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Harborview Medical Center Harborview Medical Center is the only designated Level 1 adult and pediatric...
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Umass Memorial Medical Center UMass Memorial Medical Center is the region's trusted academic medical center,...
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