Optical Coherence Tomography Angiography Assessment of Retinal Lesions in Inflammatory Bowel Diseases
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ClinicalTrials.gov Identifier: NCT04601805 |
Recruitment Status :
Not yet recruiting
First Posted : October 26, 2020
Last Update Posted : October 26, 2020
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Condition or disease | Intervention/treatment |
---|---|
Inflammatory Bowel Diseases | Device: Observation |
a prospective study of 30 patients suffering from IBD referred from tropical department from Tanta University Hospital
-Patients demographic data e.g., sex, age, concomitant systemic diseases will be recruited. Presenting symptoms, physical examination results, laboratory and imaging findings, and received treatment of IBD will be recorded. Accurate grading of disease severity will be carried out by gastroenterology specialist.
All patients will be subject to Full ophthalmologic examination and fundus imaging. Imaging will include OCTA and fundus photography. OCTA will be performed using cirrus OCT (Zeiss, Inc., USA). High-quality 6 x 6 mm OCTA macular scans and 3 × 3-mm papillary scan with strong signal-noise ratio and adequate centration on the fovea and optic nerve head respectively will be selected. Segmentation will be used to evaluate superficial and deep capillary retinal plexus projections in addition to the choriocapillaries. If errors in segmentation were detected, manual correction would be performed. The superficial retinal capillary plexus (SCP) will be delineated with an inner boundary at the internal limiting membrane (ILM) and an outer boundary 10 µm inside the inner plexiform layer (IPL). The deep retinal capillary plexus (DCP) will be segmented with an inner boundary 10 µm inside the IPL and an outer boundary at 10 µm beneath the outer plexiform layer (OPL).
The vessel density metric from enface OCT angiogram will be used as an indicator of macular retinal and papillary perfusion. Vessel density (VD) analysis computes the percentage of area occupied by OCTA detected vasculature in a measured area. Choriocapillaries flow voids will be computed to assess choriocapillaries circulation
Study Type : | Observational [Patient Registry] |
Estimated Enrollment : | 30 participants |
Observational Model: | Other |
Time Perspective: | Prospective |
Target Follow-Up Duration: | 1 Month |
Official Title: | Optical Coherence Tomography Angiography Assessment of Retinal Lesions in Inflammatory Bowel Diseases |
Estimated Study Start Date : | November 1, 2020 |
Estimated Primary Completion Date : | March 31, 2021 |
Estimated Study Completion Date : | July 29, 2021 |
Group/Cohort | Intervention/treatment |
---|---|
Group (1) : Patient diagnosed with IBD with no treatment received |
Device: Observation
We will record the vascular changes that follow the inflammatory bowel diseases |
Group(2): Patient diagnosed with IBD and received treatment for a long time |
Device: Observation
We will record the vascular changes that follow the inflammatory bowel diseases |
- vascular changes in the posterior segment of patients suffering from inflammatory bowel disease using the optical coherence tomography angiography [ Time Frame: 1 month ]
OCTA will be performed using cirrus OCT (Zeiss, Inc., USA). High-quality 6 x 6 mm OCTA macular scans and 3 × 3-mm papillary scan with strong signal-noise ratio withadequate centration on the fovea and optic nerve head Segmentation will be used to evaluate superficial and deep capillary retinal plexus projections in addition to the choriocapillaries. The superficial retinal capillary plexus (SCP) will be delineated with an inner boundary at the internal limiting membrane (ILM) and an outer boundary 10 µm inside the inner plexiform layer (IPL). The deep retinal capillary plexus (DCP) will be segmented with an inner boundary 10 µm inside the IPL and an outer boundary at 10 µm beneath the outer plexiform layer (OPL).
The vessel density metric from enface OCT angiogram as an indicator of macular retinal and papillary perfusion.

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Ages Eligible for Study: | 15 Years to 50 Years (Child, Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Patients with Crohn's disease and ulcerative colitis either newly diagnosed or suffering from chronic disease on treatment will be included
Exclusion Criteria:
-
Recent ophthalmological surgery.
- Low quality ophthalmological exams.
- Refractive errors greater than + 3 or - 3 spherical.
- Retinopathies such as diabetic retinopathy.
- Any type of retinal degenerations or retinal dystrophy.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04601805
Contact: Dina SM Tadros, MD | 00201224093354 | dinasabry@rocketmail.com |
Responsible Party: | Dina Tadros, Lecturer of Ophthalmology, Tanta University, Egypt, Tanta University |
ClinicalTrials.gov Identifier: | NCT04601805 |
Other Study ID Numbers: |
34002/8/20 |
First Posted: | October 26, 2020 Key Record Dates |
Last Update Posted: | October 26, 2020 |
Last Verified: | October 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | Yes |
Product Manufactured in and Exported from the U.S.: | No |
Intestinal Diseases Inflammatory Bowel Diseases Gastrointestinal Diseases Digestive System Diseases Gastroenteritis |