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The Effect of Hyperbaric Chamber Treatment on Patients With Diabetic Retinopathy

The Effect of Hyperbaric Chamber Treatment on Patients With Diabetic Retinopathy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02235935
Enrollment
40
Registered
2014-09-10
Start date
2014-09-30
Completion date
2016-09-30
Last updated
2014-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Does Hyperbaric Chaber Treatment Improve Diabetic Retinopathy

Brief summary

Diabetic retinopathy (DR) is a common complication of diabetes and is divided into non proliferative DR and proliferative DR. The damage is caused by either macular edema, macular ischemia that can be followed by vascular proliferation. Hyperbaric chamber treatment assists in increasing the amount of oxygen in the plasma and in the tissues and has been proven to be beneficial in treating different wounds in diabetic patients but its effect hasn't been tested in diabetic retinopathy yet. This study will recruit 40 diabetic patients who are scheduled for hyperbaric treatment due to different indications such as chronic wounds or radiation damages and who also have diabetic retinopathy. These patients will undergo opthalmic physical examination including fundus photography and OCT (Optical Coherence Tomography - optical IR retinal photography). Screening for these patients will be conducted at the Hyperbaric chamber at Assaf Harofe Medical Center for all diabetic patients prior to their first treatment.

Interventions

None listed

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion criteria: 1. Patients between ages 18-90 with Diabetes type I or II and diabetic retinopathy who are scheduled for hyperbaric treatment for other indications than DR. 2. Patients who signed an informed consent form and agree to undergo an ophthalmic physical examination, Fundus photography and OCT prior to hyperbaric treatment and oCT exam following every 10 treatments in hyperbaric chamber. Total number of hyperbaric treatments will be conducted according to the main indication for which they have been assigned this treatment.

Exclusion criteria

1. Patients with Carotid stenosis of more than 70% 2. Anemia of \< 10mg/Dl 3. Patients with chest X ray pathology which cannot be admitted to hyperbaric chamber treatment. 4. Patients with claustrophobia or that cannot decompress properly. 5. Patients with any malignant disease 6. Patients with inability to sign informed consent Decompression treatment will last 90 minutes in 2 atmospheres pressure with 100% oxygen. \-

Design outcomes

Primary

MeasureTime frameDescription
OCT results1 monththe reduction in retina width as recorded on OCT following 20 treatments in Hyperbaric Chamber

Secondary

MeasureTime frameDescription
Visual Acuity1 monthchanges in visual acuity as recorded in ophthalmologic exam before and after treatments in hyperbaric chamber

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026