NCT03222362

Brief Summary

We reviewed the records of 120 consecutive patients (male and female), aged 85 years and above, who underwent pars plana vitrecromy in the Tel Aviv Medical Center during the years 01/01/2006 - 31/12/2013, and were followed by physicians in the ophthalmology department in the center until December 2015.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2006

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2006

Completed
8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2013

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2015

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

July 16, 2017

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 19, 2017

Completed
Last Updated

July 19, 2017

Status Verified

July 1, 2017

Enrollment Period

8 years

First QC Date

July 16, 2017

Last Update Submit

July 16, 2017

Conditions

Vitreous InjuryRetinal DetachmentAge Related Macular Degeneration

Keywords

retinal detachmenttraumaage related macular degeneration

Outcome Measures

Primary Outcomes (1)

  • visual acuity

    visual acuity in Snellen chart

    study entry until December 2015 .

Secondary Outcomes (1)

  • Postoperative complications

    study entry until December 2015 .

Study Arms (1)

patients 85 years and above

120 consecutive patients (male and female), aged 85 years and above, who underwent pars plana vitrecromy in the Tel Aviv Medical Center during the years 01/01/2006 - 31/12/2013, and were followed by physicians in the ophthalmology department in the center until December 2015.

Other: Surgery

Interventions

SurgeryOTHER
patients 85 years and above

Eligibility Criteria

Age85 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients aged 85 years and above, who underwent pars plana vitrecromy in the Tel Aviv Medical Center during the years 01/01/2006 - 31/12/2013

You may qualify if:

  • Patients aged 85 years and above, who underwent pars plana vitrecromy in the Tel Aviv Medical Center during the years 01/01/2006 - 31/12/2013

You may not qualify if:

  • ANy other

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Retinal DetachmentMacular DegenerationWounds and Injuries

Interventions

Surgical Procedures, Operative

Condition Hierarchy (Ancestors)

Retinal DiseasesEye DiseasesRetinal Degeneration

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head Of vitrerretinal service

Study Record Dates

First Submitted

July 16, 2017

First Posted

July 19, 2017

Study Start

January 1, 2006

Primary Completion

December 31, 2013

Study Completion

December 31, 2015

Last Updated

July 19, 2017

Record last verified: 2017-07