Treatment of Malignant Glaucoma by Anterior Vitrectomy From Two Different Approaches

Sponsor
Wenzhou Medical University (Other)
Overall Status
Completed
CT.gov ID
NCT04172857
Collaborator
(none)
9
45

Study Details

Study Description

Brief Summary

To compare the surgical outcomes of treating phacoemulsification with intraocular lens implantation combined with goniosynechialysis (Phaco-IOL-GSL) associated malignant glaucoma (MG), using different incision sites in anterior vitrectomy combined with hyaloidotomy, zonulectomy, and iridectomy (VHZI).

Condition or Disease Intervention/Treatment Phase
  • Procedure: anterior vitrectomy combined with hyaloidotomy, zonulectomy and iridectomy

Study Design

Study Type:
Observational
Actual Enrollment :
9 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Treatment of Malignant Glaucoma Secondary to Cataract Surgery Combined With Goniosynechialysis by Anterior Vitrectomy From Two Different Approaches
Actual Study Start Date :
May 1, 2015
Actual Primary Completion Date :
Jan 20, 2019
Actual Study Completion Date :
Jan 30, 2019

Outcome Measures

Primary Outcome Measures

  1. Relapse of MG [follow up: 3 to 31 months]

    MG relapse after the anterior vitrectomy combined with hyaloidotomy, zonulectomy, and iridectomy (VHZI).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • MG was diagnosed based on the presence of a central and peripheral shallow anterior chamber with normal or elevated intraocular pressure (IOP).
Exclusion Criteria:
  • The diagnosis was made only after confirming the absence of choroidal detachment or hemorrhage and posterior segment mass lesion, using B-scan ultrasonography or ophthalmoscopy

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Wenzhou Medical University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
yin ying zhao, Researcher;clinical research center, Wenzhou Medical University
ClinicalTrials.gov Identifier:
NCT04172857
Other Study ID Numbers:
  • QZB-MG
First Posted:
Nov 21, 2019
Last Update Posted:
Nov 21, 2019
Last Verified:
Nov 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 21, 2019