Hyperbaric Oxygen and Fibromyalgia: Randomised Prospective Clinical Trial
Primary Purpose
Fibromyalgia
Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Hyperbaric oxygen
Sponsored by
About this trial
This is an interventional treatment trial for Fibromyalgia focused on measuring hyperbaric oxygen, fibromyalgia, chronic pain syndrome
Eligibility Criteria
Inclusion Criteria:
- fibromyalgia diagnosed by physical examination of pain sensitivity, by Dolorimeter and finger pressure.
Exclusion Criteria:
- any past hyperbaric oxygen therapy
- chest x-ray pathology which does not allow the income into the hyperbaric chamber.
- middle ear problems.
- patients, who cannot "pump", equals middle ear pressure, effectively.
- patients who suffer from claustrophobia.
- inability or Refusing to sign the Informed Consent Form
Sites / Locations
- Hyperbaric unit, Assaf- Harofe Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Other
Arm Label
Hyperbaric oxygen therapy group
Crossed group
Arm Description
hyperbaric oxygen therapy during the first 2 months
no active intervention during the first 2 months.After 2 months will be crossed to HBOT
Outcomes
Primary Outcome Measures
Pain evaluation
Secondary Outcome Measures
Quality of Life
Brain SPECT scan
Full Information
NCT ID
NCT01827683
First Posted
April 6, 2011
Last Updated
April 8, 2013
Sponsor
Assaf-Harofeh Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01827683
Brief Title
Hyperbaric Oxygen and Fibromyalgia: Randomised Prospective Clinical Trial
Official Title
The Effect of Hyperbaric Oxygen on Patients Suffering From Chronic Pain Syndrome (Fibromyalgia)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assaf-Harofeh Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of the study is to evaluate the effect of hyperbaric oxygen therapy (HBOT) on patients suffering from chronic pain syndrome (Fibromyalgia).
Detailed Description
The study is a prospective, randomized, cross-over trial. Patients will be randomized into two groups (test and control) to receive the HBOT at the beginning of the trial or 2 months afterwards. The control group will receive its treatment after the elapsed two months.
This study will be a prospective, randomized cross over study. After signing a written informed consent, all patients will be invited to a 2 hour examination, including pain sensitivity examination and a series of questionnaires. In addition, prior to the beginning of the treatment all patients will have chest X-ray, neurological examination, cognitive evaluation and brain metabolism evaluation (SPECT scan). A similar evaluation will be done after the 8 weeks, test versus control time period, and another evaluation will be held after 16 weeks. The HBOT procedure will be performed in the hyperbaric chamber at Assaf Harofeh Medical Center, Israel.
The following HBOT protocol will be applied for the treated group: 8-week, 5 times a week administration of 100% O2 for 90 minutes at a pressure of 2 ATA. After 8 weeks the control group, that did not received HBOT, will receive the same HBOT protocols.
At baseline, after 2 months and after 4 months all patients will undergo complete neurologic and pain evaluation and brain SPECT scan (total of 3 evaluation and scan per patient).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
hyperbaric oxygen, fibromyalgia, chronic pain syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hyperbaric oxygen therapy group
Arm Type
Active Comparator
Arm Description
hyperbaric oxygen therapy during the first 2 months
Arm Title
Crossed group
Arm Type
Other
Arm Description
no active intervention during the first 2 months.After 2 months will be crossed to HBOT
Intervention Type
Other
Intervention Name(s)
Hyperbaric oxygen
Intervention Description
8-week, 5 times a week administration of 100% O2 for 90 minutes at a pressure of 2 ATA.
Primary Outcome Measure Information:
Title
Pain evaluation
Time Frame
up to 4 months
Secondary Outcome Measure Information:
Title
Quality of Life
Time Frame
0,2,4 months
Title
Brain SPECT scan
Time Frame
0,2,4 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
fibromyalgia diagnosed by physical examination of pain sensitivity, by Dolorimeter and finger pressure.
Exclusion Criteria:
any past hyperbaric oxygen therapy
chest x-ray pathology which does not allow the income into the hyperbaric chamber.
middle ear problems.
patients, who cannot "pump", equals middle ear pressure, effectively.
patients who suffer from claustrophobia.
inability or Refusing to sign the Informed Consent Form
Facility Information:
Facility Name
Hyperbaric unit, Assaf- Harofe Medical Center
City
Zerifin
ZIP/Postal Code
70300
Country
Israel
12. IPD Sharing Statement
Citations:
PubMed Identifier
26010952
Citation
Efrati S, Golan H, Bechor Y, Faran Y, Daphna-Tekoah S, Sekler G, Fishlev G, Ablin JN, Bergan J, Volkov O, Friedman M, Ben-Jacob E, Buskila D. Hyperbaric oxygen therapy can diminish fibromyalgia syndrome--prospective clinical trial. PLoS One. 2015 May 26;10(5):e0127012. doi: 10.1371/journal.pone.0127012. eCollection 2015.
Results Reference
derived
Learn more about this trial
Hyperbaric Oxygen and Fibromyalgia: Randomised Prospective Clinical Trial
We'll reach out to this number within 24 hrs