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Studying the effect of a new type of honey eye drop on dry eye patients

Studying the effect of a new type of honey eye drop on dry eye in patients with dry eye

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220117053744N1
Enrollment
80
Registered
2023-04-16
Start date
2022-12-22
Completion date
Unknown
Last updated
2023-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

dry eye syndrom. Other disorders of lacrimal gland

Interventions

Intervention 1: Intervention group: treatment with honey drops (prepared from Gavan honey, produced by "Kandu Asal" company
1% honey in Tearlose drops)
Three times a day, one drop each time for one month, (routine treatment of dry eyes will not be removed for this group of patients). Intervention 2: Control group: Standard treatment includes artifici

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients (male or female, without age limit) with dry eye syndrome (at three levels of low, moderate, and severe) Best corrected vision greater than or equal to 9/10 Schirmer test is less than 5 mm in 5 minutes Tear break time is less than 10 seconds

Exclusion criteria

Exclusion criteria: Patients with blepharitis disorder Patients with meibomian gland disorder Patients with a history of taking tetracycline for the past three months Patients with a history of taking oral corticosteroids for the past three months Patients with ocular surface disorders Patients with a history of previous surgery Patients with a history of allergies

Design outcomes

Primary

MeasureTime frame
Tear break up time (TBUT). Timepoint: 2, 4 and 6 weeks after starting treatment. Method of measurement: Clinical examination of the patient - per second.;Corneal staining. Timepoint: 2, 4 and 6 weeks after starting treatment. Method of measurement: Clinical examination of the patient with Fluorescein test.;Basic tear secretion rate. Timepoint: 2, 4 and 6 weeks after starting treatment. Method of measurement: Clinical examination of the patient - In millimeters per minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Khaki

Shiraz University of Medical Sciences

mehdikhaki1989@yahoo.com+98 901 043 0859

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026