Lubricating Effectiveness of Carragelose Eye Drops in Patients Affected by Mild to Moderate Dry Eye

NCT ID: NCT06262100

Last Updated: 2024-12-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-01-15
• Study Completion Date: 2024-07-30

Brief Summary

Patients suffering from dry eye syndrom will treat their eyes with Carragelose® eye drops three times a day for 28 days. Before, in the middle and at the end of the treament period patients will be exposed to adverse conditions to challenge dry eye symptoms. Patient will record their occular symptoms and ophthalmic examinations will be performed by an ophthalmologist. Differences between before and after treatment will be assessed.

Detailed Description

The objective is to evaluate the safety and performance of Carragelose®-containing eye drops in treating symptoms and signs of dry eye syndrom.

Patients will treat their eyes with one eye drop three times a day for 28 days. Baseline assessment will be performed after normal controlled environment and after adverse controlled environment. At the end of investigation ocular symptoms and ocular sign will be assessed after normal controlled environment and after adverse controlled environment. Differences between baseline and end of investigation will be evaluated for efficacy analysis.

Conditions

Dry Eye Syndromes

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Carragelose

Treatment with Carragelose containing eye drops

Group Type: OTHER

Carragelose

Intervention Type: DEVICE

Application of Carragelose containing eye drops

Interventions

Carragelose

Application of Carragelose containing eye drops

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Adult patients (aged ≥ 18 years) from any sex or gender who provide written informed consent to participate.

2. Diagnosis of DED by an ophthalmologist having DED-related symptoms lasting at least 3 months.

3. Mild-to-moderate DED as defined above.

4. Patients who do not use or can do without the use of contact lenses from at least 7 (±2) days before the Inclusion visit (Visit 2) and throughout the entire study period.

5. Patients able to administer the study eye drops themselves in both eyes for the intended duration of the study (28 days).

6. Patients willing not to use any other eye drops during the entire study period.

7. Women with childbearing potential must commit to using effective methods of contraception during the entire study period and have a negative result on a pregnancy test at the Screening visit.

Exclusion Criteria

1. Patients with known hypersensitivity, allergy, or intolerance to the IP or any of its components.

2. Patients with any ocular surface disease or condition other than DED.

3. Patients with any other active ocular inflammatory disease or condition, glaucoma or who have received any ocular surgery during the last 6 months.

4. Patients who have received lacrimal punctum occlusion during the previous month, or in whom it is planned during the study period.

5. Patients with any of the following seriousness criteria:

• fluorescein corneal staining score ≥ 4 in the Oxford scale;
• lissamine green conjunctival staining score ≥ 4 in the Oxford scale;
• Schirmer test score < 2 mm;
• fluorescein TBUT = 0 seconds.

6. Patients receiving any other topical ocular medication, such as non-steroidal anti-inflammatory drugs, etc. within 30 days of inclusion (Visit 2).

7. Patients with clinically relevant or uncontrolled systemic diseases (except for controlled Sjögren syndrome) during the last 3 months that may interfere with study assessments or results.

8. Patients requiring or who have received topical ocular treatment with calcineurin inhibitors (such as cyclosporin or tacrolimus) during the last 12 weeks, corticosteroids during the last 4 weeks, blood derivatives (such as autologous/allogeneic serum, platelet-rich plasma, plasma rich in growth factors or umbilical cord-derived plasma), insulin or amniotic membrane preparations during the last week, during the last month before the Inclusion visit (Visit 2).

9. Patients who have received treatment with any ocular lubricant after the Screening visit (Visit 1) other than the one specified in the protocol (Hydrabak).

10. Patients who have started systemic treatments that may affect DED signs or symptoms, ocular surface or vision, during the last 3 months or if a change in the dose of such treatments is expected during the study.

11. Inability to follow the study procedures, including attending all site visits, tests, and examinations.

12. Mental incapacity that precludes adequate understanding or cooperation.

13. Patients currently participating or who have participated in another investigational study during the last 30 days.

14. Pregnant or breastfeeding women.

15. Patients who, according to the investigator's criteria, are not suitable to participate in the study or comply with the study protocol.

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• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Marinomed Biotech AG

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Margarita Calogne, PhD

Role: PRINCIPAL_INVESTIGATOR

IOBA, University of Valladolid

Locations

IOBA,Ocular Surface Research Group, University of Valladolid

Valladolid, , Spain

Countries

Spain

Other Identifiers

EYL_23_01

Identifier Type: -

Identifier Source: org_study_id