Hyperbaric Oxygen Therapy Induced Neuroplasticity in Post Stroke Patients Suffering Chronic Neurological Deficiencies

Sponsor
Assaf-Harofeh Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT00715897
Collaborator
(none)
74
2
2
39
37
0.9

Study Details

Study Description

Brief Summary

The aim of the current work was to evaluate, for the first time in a prospective randomized study, the effect of HBOT on patients with chronic neurological deficiency due to stroke.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Hyperbaric Oxygen Therapy (HBOT)
N/A

Detailed Description

Objective: Evaluate the effect of hyperbaric oxygen therapy (HBOT) on patients with chronic neurological deficiency due to stroke.

Methods: A prospective, randomized, control-crossed over trial including patients who had stroke 6-36 months prior to their inclusion. All patients had at least one motor dysfunction. After their inclusion patients were randomized to treated or cross group. The neurologic functions were evaluated by NIHSS, ADL, life quality and brain SPECT. Patients in the treated group were evaluated twice-at baseline and after HBOT. Patients in the cross group were evaluated three times-baseline, after 2 months control period of no treatment and after a consequent 2 month of HBOT. The following HBOT protocol was practice: 40 daily sessions, 90 minutes each, 100% oxygen at 2ATA, 5 days/week,.

Results: The study included 74 patients (8 were excluded). During the control period, in the cross group, NIHSS and the ADL had not changed, while in the treated group both significantly improved. After the cross-over, when the cross group received HBOT, NIHSS and ADL had significantly improved. Same trend of changes were in life quality. The SPECT correlated with the clinical improvement. The improvements were mostly in territories where there was a noticeable discrepancy between the CT and SPECT.

Interpretation: In this study, for the first time, it was demonstrated that HBOT can induce neuroplasticity in patients with chronic neurologic deficiencies due to stroke. The beneficial effect of the HBOT is mostly in territories where there is a brain SPECT/CT mismatch.

Study Design

Study Type:
Interventional
Actual Enrollment :
74 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Study Start Date :
Aug 1, 2008
Actual Primary Completion Date :
Oct 1, 2010
Actual Study Completion Date :
Nov 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment- HBOT

HBOT treatment: 8-week, 5 times a week administration of 100% O2 for 90 minutes at a pressure of 2 ATA.

Procedure: Hyperbaric Oxygen Therapy (HBOT)
8-week, 5 times a week administration of 100% O2 for 90 minutes at a pressure of 2 ATA.

No Intervention: control-HBOT

Cross group: Patients in the cross group were evaluated three times-baseline, after 2 months control period of no treatment and after a consequent 2 month of HBOT

Outcome Measures

Primary Outcome Measures

  1. Neurologic evaluation [2 and 4 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18 years or older, who had ischemic stroke and 60 patients who had hemorrhagic stroke 6-18 months prior to their inclusion in the study.
Exclusion Criteria:
  • Dynamic neurologic improvement or worsening during the last 4 weeks.

  • Had been treated with HBO for any other reason prior to their inclusion.

  • Have any other indication for HBOT

  • Chest pathology incompatible with pressure changes

  • Inner ear disease

  • Patients suffering from claustrophobia.

  • Inability to give written informed consent.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Asaf-Harofeh Medical Center Zerifin Israel 70300
2 Research & Development unit, Asaf-Harofeh Medical Center Zerifin Israel 70300

Sponsors and Collaborators

  • Assaf-Harofeh Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fany Tusia, medical center, Assaf-Harofeh Medical Center
ClinicalTrials.gov Identifier:
NCT00715897
Other Study ID Numbers:
  • HBOcva1
First Posted:
Jul 15, 2008
Last Update Posted:
Dec 26, 2011
Last Verified:
Dec 1, 2011
Keywords provided by Fany Tusia, medical center, Assaf-Harofeh Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 26, 2011