Novel Use of an Adjustable Single 8-0 Polypropylene Suture of Scleral Fixation Without Conjunctival Dissection | NCT04476264 | Trialant
CompletedObservationalUpdated Jul 20, 2020
Novel Use of an Adjustable Single 8-0 Polypropylene Suture of Scleral Fixation Without Conjunctival Dissection
Novel Use of an Adjustable Single 8-0 Polypropylene Suture of Scleral Fixation
ClinicalTrials.gov ID
NCT04476264
Lead Sponsor
Beijing Tongren HospitalOTHER
Overall Status
Completed
Study Type
Observational
Enrollment
27Actual
Last Update Posted
Jul 20, 2020Actual
Start Date
Apr 1, 2018Actual
Primary Completion Date
Apr 1, 2018Actual
Completion Date
Jul 30, 2019Actual
Official Title
Novel Use of an Adjustable Single 8-0 Polypropylene Suture of Scleral Fixation
Brief Summary
observe the effectivity of an adjustable single 8-0 polypropylene suture to scleral fix without conjunctival dissection for the treatment with aphakia or inadequate posterior capsule support.
observe the complication of this surgery method.
Suture, Complication
Novel use of an adjustable single 8-0 polypropylene suture of scleral fixation without conjunctival dissection
Ages Eligible for Study
Child (0-17)Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Any patients who used an adjustable single 8-0 polypropylene suture of scleral fixation without conjunctival dissection could be included.
Exclusion Criteria:
Data from patients with a < 6-month postoperative follow-up or with incomplete operative or postoperative medical records were excluded from this study. Enrolled patients had complete records pertaining to their visual acuity (VA), slit-lamp photographs, and ultrasound biomicroscope (UBM) findings.