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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02890888
Other study ID # 2014.011
Secondary ID
Status Terminated
Phase N/A
First received September 5, 2014
Last updated October 25, 2017
Start date November 2014
Est. completion date October 25, 2017

Study information

Verified date October 2017
Source St. Luke's Hospital, Chesterfield, Missouri
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients will have a Functional MRI before and after 10 hyperbaric Oxygen treatments.


Description:

Functional MRI studies will be done before and 4-6 weeks after Hyperbaric Oxygen treatment to assess changes in connectivity of resting state neural networks. 10 hyperbaric treatments at 2 atmospheres absolute for 1 hour at pressure will be administered. A review of symptoms and and thorough clinical neurological examination by an experienced neurologist familiar with these studies will be done before and 4-6 weeks after the hyperbaric treatments.


Recruitment information / eligibility

Status Terminated
Enrollment 6
Est. completion date October 25, 2017
Est. primary completion date October 25, 2017
Accepts healthy volunteers No
Gender All
Age group 50 Years to 90 Years
Eligibility Inclusion Criteria:

- White Matter Hyperintensities on MRI

- 2 or more neurological symptoms or impairments e.g. gait disturbances, disequilibrium, cognitive decline, dysmetria, hyper-rflexia

Exclusion Criteria:

- Contraindication to hyperbaric oxygen treatment e.g. pulmonary emphysema, seizure disorder

- major eustachian tube dysfunction

- stroke with previous 6 months

- extreme cognitive impairment

- major depression

- history of migraine, electroshock therapy, brain irradiation, brain tumor, head trauma

- other uncontrolled co-morbidities, e.g. diabetes, renal or hepatic dysfunction, hypertension, thyroid disorders, carotid artery stenosis (>70%)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
hyperbaric oxygen treatment
Patients are treated in a hyperbaric oxygen chamber for 1 hour at 2ATA, 10 times over 2 consecutive weeks, 5 times per week

Locations

Country Name City State
United States St. Luke's hospital Chesterfield Missouri
United States Mallinckrodt Institute of Radiology/Washington University Medical School Saint Louis Missouri
United States St. Luke's Hospital Saint Louis Missouri

Sponsors (2)

Lead Sponsor Collaborator
St. Luke's Hospital, Chesterfield, Missouri Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in average functional connectivity (fc) within the Default Mode Network and the Dorsal Attention Network will be obtained by resting state network (rsn) functional connectivity (rsnfc) MRI. Functional connectivity MRI of resting state neural networks. Change in baseline rsnfc before and 4 weeks after hyperbaric oxygen
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