Clinical Study of the Effect of Intravenous Galactose on Diabetic Macular Oedema
Primary Purpose
Diabetic Macular Oedema
Status
Terminated
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Galactose, intravenous
Sponsored by
About this trial
This is an interventional treatment trial for Diabetic Macular Oedema focused on measuring Diabetes, Macular oedema, Osmosis, Galactose, Intravenous, Retinal thickness, Starling
Eligibility Criteria
Inclusion Criteria:
- Type 1 or type 2 diabetes
- clinically significant macular oedema
- visual acuity of minimum 40 letters by the ETDRS procedure
- retinal thickness of at least 250 microns in the foveal region on three retinal maps of the fast protocol of the StratusOCT at baseline or at least 300 microns outside the foveal region
- 1 disc area of oedema within 3000 microns from the foveal center on three retinal maps of the fast protocol of the StratusOCT at baseline
- maximal blood pressure 160/90 mmHg (mean of three measurements)
- informed consent
Exclusion Criteria:
- other ocular diseases or treatments, that can cause or influence the macular oedema, including prior laser photocoagulation. Traction oedema is allowed.
- glaucoma
- media opacities that significantly impairs the light reflection while scanning
- Pregnancy
- severe heart, lung and/or renal insufficiency (judged by the primary investigator)
Sites / Locations
- Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Nordre Ringvej 57,
Outcomes
Primary Outcome Measures
Retinal thickness estimated by the fast protocol of the StratusOCT (0, 2, 4, 8, 10, 15, 20, 30, 60, 90, 120 and 180 min).
Secondary Outcome Measures
Side effects during the three-hour examination period, to evaluate if caused by galactose per se or by an increase in intracapillary osmotic pressure.
Full Information
NCT ID
NCT00427986
First Posted
January 25, 2007
Last Updated
June 25, 2007
Sponsor
Glostrup University Hospital, Copenhagen
1. Study Identification
Unique Protocol Identification Number
NCT00427986
Brief Title
Clinical Study of the Effect of Intravenous Galactose on Diabetic Macular Oedema
Official Title
Diabetic Macular Oedema: Quantification of the Effect of Rising the Intracapillary Osmotic Pressure With Intravenous Galactose on the Retinal Thickness
Study Type
Interventional
2. Study Status
Record Verification Date
June 2007
Overall Recruitment Status
Terminated
Why Stopped
No sufficient increase in plasma osmolarity by galactose (one patient included)
Study Start Date
January 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Glostrup University Hospital, Copenhagen
4. Oversight
5. Study Description
Brief Summary
The purpose of the present study is to examine, if retinal swelling in diabetic patients can be reduced by an intravenous injection of galactose.
Detailed Description
Macular oedema (swelling of the retina) is a leading cause of severe visual loss and blindness in patients with diabetes. The oedema is caused by fluid accumulation in the retinal tissue from leaking capillaries and leads to an increase in the retinal thickness. Optical Coherence Tomography (OCT) has become the primary technique to estimate the retinal thickness objectively, and the scans can be performed without any discomfort to the patient after dilation of the pupils.
According to the Starling equation, a general basic physiologic rule, specific factors influence the fluid transport between the capillaries and the surrounding tissue. One of these factors is the balance between the large molecules within the vessel lumen and the surrounding tissue, e.g. the osmotic pressure balance. By changing the osmotic balance some drugs can reduce the fluid content in the tissue by extracting water from the tissue to the vessel lumen. Such a drug is galactose.
In the present study we examine, if treatment with intravenous galactose can reduce the retinal thickness in diabetic macular oedema evaluated by OCT during a three-hour monitoring. Galactose (0.5 mg/mL) is administered as 1 mL galactose per kg body weight + 10% with a maximum of 80 mL, and injection time is 5 min. If reduction of the thickness with galactose is found, it then confirms the application of the Starling osmotic forces on diabetic macular oedema. In the same time span series of venous blood samples are taken for analysis of plasma osmolarity and electrolytes. The systemic blood pressure is also monitored as well as the capillary glucose level.
As diurnal variations in the retinal thickness estimates potentially can influence the results, the OCT measurements and blood samples are repeated on a second day for each participant, without treatment with galactose for comparison. The order of two visits is given by randomisation.
Interim analysis will take place after inclusion of 15 to 20 patients to evaluate the need for inclusion of 45 patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Macular Oedema
Keywords
Diabetes, Macular oedema, Osmosis, Galactose, Intravenous, Retinal thickness, Starling
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Galactose, intravenous
Primary Outcome Measure Information:
Title
Retinal thickness estimated by the fast protocol of the StratusOCT (0, 2, 4, 8, 10, 15, 20, 30, 60, 90, 120 and 180 min).
Time Frame
three hours
Secondary Outcome Measure Information:
Title
Side effects during the three-hour examination period, to evaluate if caused by galactose per se or by an increase in intracapillary osmotic pressure.
Time Frame
Three hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 1 or type 2 diabetes
clinically significant macular oedema
visual acuity of minimum 40 letters by the ETDRS procedure
retinal thickness of at least 250 microns in the foveal region on three retinal maps of the fast protocol of the StratusOCT at baseline or at least 300 microns outside the foveal region
1 disc area of oedema within 3000 microns from the foveal center on three retinal maps of the fast protocol of the StratusOCT at baseline
maximal blood pressure 160/90 mmHg (mean of three measurements)
informed consent
Exclusion Criteria:
other ocular diseases or treatments, that can cause or influence the macular oedema, including prior laser photocoagulation. Traction oedema is allowed.
glaucoma
media opacities that significantly impairs the light reflection while scanning
Pregnancy
severe heart, lung and/or renal insufficiency (judged by the primary investigator)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dorte Nellemann Thornit, MD
Organizational Affiliation
Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Nordre Ringvej 57, DK-2600 Glostrup, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Nordre Ringvej 57,
City
Glostrup
ZIP/Postal Code
DK-2600
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Clinical Study of the Effect of Intravenous Galactose on Diabetic Macular Oedema
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