Angiogenesis Induced in the Elderly by Hyperbaric Oxygen Therapy (ANGIOHBOT)

January 3, 2020 updated by: Assaf Harofeh MC, Assaf-Harofeh Medical Center

Changes in Blood Flow and Angiogenesis Induced in the Elderly by Hyperbaric Oxygen Therapy

Recent studies show preliminary evidence of HBOT therapeutic effects on angiogenesis, increased tissue blood flow and oxygenation correlated with tissue function.

Our primary hypothesis is that HBOT will have beneficial effects on the above mentioned organs associated with aging-related malfunctions due to restored mitochondrial function, mobilization of stem cells and induction of angiogenesis.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The paradigm The accumulation of damage to molecules, cells and tissues over a lifetime that contributes to aging eventually leads to frailty and malfunction. The past decade has seen fundamental advances in our understanding of the aging process and raised optimism that interventions to slow ageing may be on the horizon. The aging process is linked to energy deficit due to tissue hypoxia and mitochondria dysfunction.

  • Mitochondria dysfunction- Mitochondria are the primary generator of energy by means of ATP synthesis and their dysfunction leads to cellular function decline and degenerative changes. In addition, mitochondria dysfunction in stem cells decreases the capabilities for tissue regeneration.
  • Tissue hypoxia- Atherosclerosis is a chronic inflammatory response that damages arterial blood vessels. It begins in childhood and progresses throughout life. A vicious cycle occurs as mitochondrial dysfunction accelerates atherosclerosis and the waning of microvasculature, resulting in decrease blood supply and ensuing relative tissue hypoxia. The decrease oxygen supply to the mitochondria further exacerbates mitochondrial dysfunction.

Hyperbaric oxygen can increase the partial pressure of dissolved (non-hemoglobin-bound) oxygen 20-30 fold and produce two main effects. First, it can eliminate the relative tissue hypoxia induced by atherosclerosis. Second, because mitochondria function is directly influenced by the partial pressure of dissolved oxygen, hyperbaric oxygen can amend mitochondrial dysfunction. Thus, the investigators suggest hyperbaric oxygen as a novel method for breaking the vicious cycle of degeneration and perhaps even for reversing the aging process.

The study is designed as a prospective crossover study aiming to evaluate the therapeutic effects of HBOT on the Brain, Cardiovascular and Immune system, Skin, Erectile (sexual functions), liver and Kidneys, of aging population.

After signing an informed consent form, patients will be invited for baseline evaluations. All patients would be evaluated 3 times - at baseline, after 3 months of follow up, and after additional 3 months of HBOT protocol. The evaluation will include cognitive assessment, questionnaires, MRI scans, blood tests and skin photograph and biopsy. In addition, blood tests will be drawn before and after the 20th, 40th and the 60th sessions for stem cells and mitochondria tests.

Patients will receive 60 daily sessions, 5 days/week, 90 minutes each with 5 minutes air break every 30 minutes, 100% oxygen at 2 ATA.

Study Type

Interventional

Enrollment (Actual)

62

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Zerifin, Israel, 70300
        • Asaf Harofeh Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age≥ 65 years
  • Capability to sign informed consent.
  • No cardiac or cerebrovascular ischemia previous events one year prior to inclusion.

Exclusion Criteria:

  • Previous treatment with HBOT for any other reason during the last 3 months prior to inclusion.
  • Any history of malignancy during the last year prior to inclusion.
  • Severe cognitive decline (MMSA<17)
  • Severe chronic renal failure (GFR <30)
  • Uncontrolled diabetes mellitus (HbA1C>8, fasting glucose>200)
  • Immunosuppressant from any reason
  • Contraindications to perform MRI: claustrophobia, allergy to gadolinium, foreign bodies, pacemaker, etc.
  • Active Smoking.
  • Pulmonary diseases such as severe emphysema, moderate-severe obstructive disease.
  • Medical conditions deemed by the investigator to make the patient ineligible for protocol investigations.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Treatment
Hyperbaric Oxygen Therapy: 3 months of treatment consisting of 60 daily sessions, 90 minutes of 100% oxygen at pressure of 2 ATA each, five days a week
60 daily sessions, 90 minutes of 100% oxygen at pressure of 2 ATA each, five days a week for 3 months.
Other Names:
  • HBOT
OTHER: Control/Crossover
Hyperbaric Oxygen Therapy: 3 months control period (no treatment) followed by 3 months of treatment consisting of 60 daily sessions, 90 minutes of 100% oxygen at pressure of 2 ATA each, five days a week
60 daily sessions, 90 minutes of 100% oxygen at pressure of 2 ATA each, five days a week for 3 months.
Other Names:
  • HBOT

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline of Angiogenesis in brain MRI at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
imaging will be performed for evaluation of brain changes and angiogenesis processs using MRI perfusion (DSC)
at baseline, 3 and 6 months
Change from baseline of general cognitive functions index at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
Patients' cognitive functions will be assessed by Neurotrax computerized cognitive tests to generate the general cognitive index
at baseline, 3 and 6 months
Change from baseline of exercise VO2 MAX at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
Using a standard exercise test which includes gas analysis, the change in VO2 maxs will be assessed 3 and 6 months compared to baseline
at baseline, 3 and 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in number of circulating stem cells (CD34) at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
Blood samples will be drawn for measurements of CD34 stem cells number analyzed by FACS.
at baseline, 3 and 6 months
Change from baseline of proteinuria at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
24-hours urine will be collected from all patients for evaluation of proteinuria
at baseline, 3 and 6 months
Change from baseline of Methacetin breath test at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
All patients will undergo Methacetin breath test. Voltile CO2 levels will be compared to evaluate changes in liver function.
at baseline, 3 and 6 months
Change from baseline in bone density at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
All patients will undergo Dual-energy X-ray absorptiometry to evaluate the change bone density changes
at baseline, 3 and 6 months
Change from baseline in quality of life measured by SF-36 form at 3 and 6 months
Time Frame: at baseline, 3 and 6 months
All patients will fill SF-36 questionnaire to evaluate the change in quality of life
at baseline, 3 and 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

December 1, 2016

Primary Completion (ACTUAL)

January 1, 2020

Study Completion (ACTUAL)

January 1, 2020

Study Registration Dates

First Submitted

May 3, 2016

First Submitted That Met QC Criteria

June 3, 2016

First Posted (ESTIMATE)

June 6, 2016

Study Record Updates

Last Update Posted (ACTUAL)

January 6, 2020

Last Update Submitted That Met QC Criteria

January 3, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 0172-15-ASF

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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