HBO: The Use of Hyperbaric Oxygen to Increase the Blood Supply in the Injured, But Still Alive Tissue, Around an Old Stroke

Sponsor
John Davidson (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01985100
Collaborator
Washington University School of Medicine (Other)
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10.2
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Study Details

Study Description

Brief Summary

To confirm or refute recently published data regarding the reduction in post-stroke ischemic penumbra, that used SPECT/CT, by using the more precise tools of PET/MRI.

Condition or Disease Intervention/Treatment Phase
  • Other: hyperbaric oxygen chamber
N/A

Detailed Description

Most patients who suffer an acute ischemic stroke improve over the immediately ensuing 30-90 days. However, many patients do not improve beyond this initial period in spite of continued intensive physical therapy and supportive care. A prospective, randomized trial of the use of hyperbaric oxygen treatments in 59 such patients was published in January 2012. That study which used 40 hyperbaric oxygen treatments, indicated significant clinical neurological improvement in residual motor deficit in patients who had sustained a stroke over a year previously. An increase in brain activity in the region immediately surrounding their stroke (penumbra) was reported on the basis of SPECT studies. Regions of live cells were determined by CT. Because SPECT is primarily a measure of perfusion and not metabolic activity and CT is a poor measure of cell life, the investigators plan to assess areas of physiologic/anatomic mismatch in similar patients following hyperbaric oxygen treatment by the use of the more appropriate and precise tools, PET and MRI.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Hyperbaric Oxygen in the Reduction of Post Stroke Ischemic Penumbra
Actual Study Start Date :
Nov 21, 2013
Actual Primary Completion Date :
Sep 27, 2014
Actual Study Completion Date :
Sep 27, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: single group

single group of 6 patients will be treated with hyperbaric oxygen at 2 atmospheres absolute (ATA) for 90 minutes 5 days per week for 4 weeks (20 treatments) to see if the previously reported increase in cell metabolism following such treatment can be better documented by the more sensitive and precise method for assessing this, i.e. PET/MRI, than the previously reported SPECT/CT method

Other: hyperbaric oxygen chamber

Outcome Measures

Primary Outcome Measures

  1. Increase in cellular metabolic activity in ischemic post stroke-penumbra PET scans [2 weeks after treatment with Hyperbaric Oxygen]

Secondary Outcome Measures

  1. Change in the motor function deficit post-stroke by Physical Therapists' measurements of motor strength [2 weeks after completion of hyperbaric oxygen therapy]

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • person must have sustained an acute ischemic stroke 6-12 months prior to enrollment, exhibited clinical improvement during the initial 30-90 days post stroke, exhibited no further improvement for at least 1 month in spite of continued supportive care and physical therapy, must have at least one residual measurable motor deficit.
Exclusion Criteria:

Smoking, Contraindications to an MRI e.g. pacemaker, Contraindications to hyperbaric oxygen treatment e.g. emphysema, claustrophobia. seizure disorder, Inability to tolerate pressurization e.g. Eustachian tube dysfunction, other uncontrolled co-morbidities e.g. diabetes, hypertension, thyroid disorders, renal or hepatic dysfunction.

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Luke's Hospital Chesterfield Missouri United States 63017

Sponsors and Collaborators

  • John Davidson
  • Washington University School of Medicine

Investigators

  • Principal Investigator: John D Davidson, MD, St. Luke's Hospital St. Louis

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
John Davidson, Principal Investigator, St. Luke's Hospital, Chesterfield, Missouri
ClinicalTrials.gov Identifier:
NCT01985100
Other Study ID Numbers:
  • StLukesMO # 2013.021
First Posted:
Nov 15, 2013
Last Update Posted:
Oct 27, 2017
Last Verified:
Oct 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 27, 2017