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Novel Use of an Adjustable Single 8-0 Polypropylene Suture of Scleral Fixation Without Conjunctival Dissection

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Capital Medical University

Status

Completed

Conditions

Suture, Complication

Treatments

Procedure: Novel use of an adjustable single 8-0 polypropylene suture of scleral fixation without conjunctival dissection

Study type

Observational

Funder types

Other

Identifiers

NCT04476264
TR2019IOL

Details and patient eligibility

About

  1. 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.
  2. observe the complication of this surgery method.

Enrollment

27 patients

Sex

All

Volunteers

No Healthy Volunteers

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.

Trial design

27 participants in 1 patient group

transscleral IOL fixation
Description:
the use of a novel adjustable single 8-0 polypropylene suture for scleral fixation without conjunctival dissection
Treatment:
Procedure: Novel use of an adjustable single 8-0 polypropylene suture of scleral fixation without conjunctival dissection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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