Effect of tacrolimus drops and PRP in the treatment of chronic dry eye

Phase 2

Recruiting

• Conditions: Dry eye syndrome.; Dry eye syndrome; H04.12

• Registration Number: IRCT20211011052725N1
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 January 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

Patients over 18 years
Corneal staining
Schirmer test is less than 5 mm in 5 minutes
BUT test is less than 5 seconds.

Exclusion Criteria

Pregnancy
Lactation
Pregnancy, lactation, history of glaucoma and previous surgery and trauma
Use of eye drops other than artificial tears, and use of contact lenses.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
BUT test (Fluorescein disappears from Fornix). Timepoint: One week, one month and three months after starting treatment. Method of measurement: Clinical examination of the patient - per second.;Corneal staining. Timepoint: One week, one month and three months after starting treatment. Method of measurement: Clinical examination of the patient.;Schirmer test. Timepoint: One week, one month and three months after starting treatment. Method of measurement: Clinical examination of the patient - In millimeters per minute.