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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03685851
Other study ID # 2017-04Obs-CHRMT
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2012
Est. completion date June 30, 2017

Study information

Verified date September 2018
Source Centre Hospitalier Régional Metz-Thionville
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To study the correlation between graft size in DSAEK (Descemet Stripping Automated Endothelial Keratoplasty) and UT (ultra thin)-DSAEK type corneal transplants to the visual acuity 6 months postoperatively.


Recruitment information / eligibility

Status Completed
Enrollment 111
Est. completion date June 30, 2017
Est. primary completion date April 1, 2015
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who underwent DSAEK surgery

- Patients in department of ophthalmology between february 2012 and june 2017

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
DSAEK type corneal transplant
All surgeries were performed by the same surgeon and according to the same protocol

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Régional Metz-Thionville

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative visual acuity postoperative visual acuity in logmar Month 6
Secondary Pachymetry Measurement of the thickness of the cornea Month 6
See also
  Status Clinical Trial Phase
Completed NCT04521140 - Assessing eFficacy and Safety of DEXTENZA 0.4 mg inseRt, Following Corneal Transplant Surgery Phase 4
Completed NCT01695655 - Neovascularization Patterns in Corneal Graft Rejection N/A