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Non Interventional Study to Evaluate the Efficacy and Tolerability of Ectoin Containing Ophthalmic Solution | Clinical Trials | Clareo Health

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COMPLETEDNCT01684852

Non Interventional Study to Evaluate the Efficacy and Tolerability of Ectoin Containing Ophthalmic Solution

This is a comparative, open label, parallel group, non interventional study to further demonstrate the efficacy and tolerability of BAT04. In addition the efficacy and safety shall be compared to Hyal...

Lead sponsor: Bitop AG•5 locations•View source on ClinicalTrials.gov

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: January 29, 2026Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment64

Start dateMay 2012

Last updatedJan 29, 2026

Condition

Dry Eye Syndromes

Locations shown

Dr. Peter Otto

Bad Liebenwerda

Dr. Insa Beddermann

Duderstadt

Augenklinik mit Poliklinik

Erlangen

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 29, 2026Data synced to Clareo: April 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Non Interventional Study to Evaluate the Efficacy and Tolerability of Ectoin Containing Ophthalmic Solution

What this study is about

Clareo turns complex medical information into clear understanding you can use.

Sponsors

Related studies

Clinical Applications of Advanced Ophthalmic Imaging

Assessment of TFT by OCT in Healthy Subjects and Subjects With DES

Difference of Tear Ferning Between Women with and Without Menopausal.

Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD

Efficacy and Safety of AJU-S56 5% in Dry Eye Syndrome Patients

Trial snapshot

Condition

Locations shown

For caregivers