Condition 1: cataract. Condition 2: Dry eye disease. Other cataract Dry eye syndrome
Conditions
Interventions
Intervention 1: Intervention group: primary biometry using IOLMaster-500 and then Instilling tearlose (Sinadaro) artificial tear drop 10 minutes before second biometry in one of a patients eyes and on
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
50 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patients aged 50 to 70 years with bilateral cataract and mild to moderate Dry eye disease Informed consent to participate in the study Absence of pathologies influencing biometry such as keratoconus, corneal scar, pathologic myopia, nanophthalmus, etc Absence of prior ocular surgical history
Exclusion criteria
Exclusion criteria: Any intra- or postoperative complication occurance Patient's failure to attend follow-up visit
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Spherical equivalent. Timepoint: At the beginning of the study and one month after surgery. Method of measurement: Topcon RM8000 autorefractometer.;Anterior chamber depth. Timepoint: At the beginning of the study and one month after surgery. Method of measurement: IOL Master 500.;Axial length. Timepoint: At the beginning of the study and one month after surgery. Method of measurement: IOL Master 500.;Mean keratometry. Timepoint: At the beginning of the study and one month after surgery. Method of measurement: Topcon RM8000 autorefractometer.;Corneal astigmatism. Timepoint: At the beginning of the study and one month after surgery. Method of measurement: Topcon RM8000 autorefractometer.;Dry eye disease severity. Timepoint: before intervention. Method of measurement: Schirmer test, TBUT test, and corneal staining. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElham Soltani
Hamedan University of Medical Sciences
Outcome results
None listed