Toric Intraocular Lens (IOL) Implantation for Management of Cataracts
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorEye & ENT Hospital of Fudan University
About this trial
This study included cataract patients who underwent toric intraocular lens (IOL) implantation, which aimed to evaluate the stability and clinical visual quality of toric IOLs.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Cataract
Disqualifiers
• small pupil
zonular dehiscence
preexisting corneal pathology
glaucoma
Trial population
Cataract patients who underwent uneventful lens phacoemulsification and toric IOL implantation.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
3,000 Participants
are grouped into 1 trial groupGroup A: cataract patients implanted with toric IOLs
Trial outcomes
Primary outcomes
1
IOL rotation degree at one hour
After the pupil was dilated, the IOL axis was recorded using the same slit-lamp microscope. IOL rotation was defined as the difference between the target and final axis.
Time frame
one hour2
IOL rotation degree at one day
After the pupil was dilated, the IOL axis was recorded using the same slit-lamp microscope. IOL rotation was defined as the difference between the target and final axis.
Time frame
one day3
IOL rotation degree at three days
After the pupil was dilated, the IOL axis was recorded using the same slit-lamp microscope. IOL rotation was defined as the difference between the target and final axis.
Time frame
three days4
IOL rotation degree at one week
After the pupil was dilated, the IOL axis was recorded using the same slit-lamp microscope. IOL rotation was defined as the difference between the target and final axis.
Time frame
one weekSecondary outcomes
1
visual quality at one week
visual acuity was evaluated by OPD-Scan III aberrometer.
Time frame
one week2
visual quality at two weeks
visual acuity was evaluated by OPD-Scan III aberrometer.
Time frame
two weeks3
visual quality at one month
visual acuity was evaluated by OPD-Scan III aberrometer.
Time frame
one month4
visual quality at three months
visual acuity was evaluated by OPD-Scan III aberrometer.
Time frame
three monthsOther outcomes
1
visual acuity at one day
uncorrected distance visual acuity (UDVA) and corrected distance visual acuity (CDVA) were recorded after surgery at one day
Time frame
one day2
visual acuity at three days
uncorrected distance visual acuity (UDVA) and corrected distance visual acuity (CDVA) were recorded after surgery at three days
Time frame
three days3
visual acuity at one week
uncorrected distance visual acuity (UDVA) and corrected distance visual acuity (CDVA) were recorded after surgery at one week
Time frame
one week4
visual acuity at two weeks
uncorrected distance visual acuity (UDVA) and corrected distance visual acuity (CDVA) were recorded after surgery at two weeks
Time frame
two weeksSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov