New eye drop battle: can ectoin beat hyaluronic acid for dry eyes?
NCT ID NCT01684852
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compared two types of eye drops—ectoin (BAT04) and hyaluronic acid—for treating dry eye disease. 64 adults with mild to moderate dry eye used the drops six times daily in both eyes for 28 days. The main goal was to see how well each drop improved tear film stability, measured by tear break-up time. Results were recorded at the end of the treatment period.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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64 people
The number who actually took part.
- Start date
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May 2012
- Finished
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Nov 2012
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
primary care clinic The selection of appropriate patients for the observational study is made by the individual physician in his treatment decisions in consultation with the individual patient
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female person aged 18 years * Demonstrated mild to moderate keratoconjunctivitis sicca ( "dry eye") * Acute symptoms of dry eye: DEWS 1-3 * tear break-up time TBUT \<10s * agreement to abide by the routinely provided doctor's appointment for follow-up (reflected in the planned visits of observation plan resist) Exclusion Criteria: * inflammation of the anterior segment or trauma * Contact lens wearers * Any disease that can, in the opinion of the treating physician to affect the outcome of the study. * Patients with known intolerance to one of the substances used * Surgical procedures to the eyes in the last 6 weeks before inclusion in the trial * patients with addictive disorders or substance abuse fallow in the past 12 months, as well as persons incapable of giving consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Augenabteilung am St. Franziskus-Hospital Münster
Münster, 48145, Germany
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Augenklinik der LMU Klinikum der Universität Muenchen
München, 80336, Germany
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Augenklinik mit Poliklinik
Erlangen, 91054, Germany
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Dr. Insa Beddermann
Duderstadt, 37115, Germany
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Dr. Peter Otto
Bad Liebenwerda, 04924, Germany
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Other studies related to the condition(s) this trial covers.
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