Cognitive Profile of Patients at the Sagol Center for Hyperbaric Medicine and Research
NCT ID: NCT04287283
Last Updated: 2024-06-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
2500 participants
OBSERVATIONAL
2008-01-31
2025-12-31
Brief Summary
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The aim of this study was to retrospectively evaluate the cognitive changes before and after HBOT in different patients populations.
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Detailed Description
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Patients included if they had at least two neurocognitive tests, before and after Hyperbaric Oxygen Therapy (HBOT). The study was approved by the institutional review board of the hospital.
Patients were treated with 40-60 daily hyperbaric sessions, 5 days per week. Each session consists of 90 minutes exposure to 100% oxygen at 1.5-2 ATA.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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HBOT
Patients with chronic brain injury or cognitive complaints that have been treated with Hyperbaric oxygen therapy and underwent computerized cognitive tests before and after the treatment
Hyperbaric Oxygen
40-60 daily hyperbaric sessions, 5 days per week. Each session consists of 90 minutes exposure to 100% oxygen at 1.5-2 ATA.
Interventions
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Hyperbaric Oxygen
40-60 daily hyperbaric sessions, 5 days per week. Each session consists of 90 minutes exposure to 100% oxygen at 1.5-2 ATA.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Assaf-Harofeh Medical Center
OTHER_GOV
Responsible Party
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Prof. Shay Efrati
Prof.
Locations
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hyperbaric center Asaf harofe medical center
Rishon LeZiyyon, , Israel
Countries
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Other Identifiers
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ASF-19-0267
Identifier Type: -
Identifier Source: org_study_id
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