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Outcomes of CTAK Surgery

Outcomes of Corneal Tissue Addition for Keratoplasty (CTAK) in Patients With Ectatic Corneas

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07474870
Acronym
CTAK
Enrollment
100
Registered
2026-03-16
Start date
2026-05-01
Completion date
2031-01-01
Last updated
2026-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corneal Ectasia, Keratoconus

Keywords

CTAK, Corneal Ectasia

Brief summary

Measuring quality of vision and quality of life outcomes using a validated questionnaire in participants undergoing CTAK surgery for corneal ectasia

Detailed description

The investigators are measuring self-reported quality of vision and quality of life outcomes in participants undergoing CTAK surgery for corneal ectasia

Interventions

BEHAVIORALQuestionnaire and Physical Exam

Patient reported outcomes of CTAK surgery

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

Preoperative and postoperative questionnaire

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Corneal Ectasia and Keratoconus

Exclusion criteria

* Excessively thin cornea * Significant corneal scarring

Design outcomes

Primary

MeasureTime frameDescription
QuestionnaireOne yearPreoperative and postoperative questionnaire

Countries

United States

Contacts

CONTACTEdward Manche, MD
edward.manche@stanford.edu16504987020

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 25, 2026