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NCT07480343Enrolling by invitation

5-Year Postoperative Outcomes of Patients Who Completed the CREST Study

FIVE-YEAR POSTOPERATIVE OUTCOMES IN PATIENTS WITH OPEN-ANGLE GLAUCOMA WHO UNDERWENT BIO-INTERVENTIONAL UVEOSCLERAL OUTFLOW ENHANCEMENT SURGERY: LONG-TERM OBSERVATIONAL FOLLOW-UP FROM THE CREST STUDY (THE CREST-XT STUDY)

Source: ClinicalTrials.gov · Last updated 21 Jul 2026

Brief summary (registry, in English)

This study is designed to collect clinical data at 3, 4, and 5 years postoperatively for participants who completed the CREST Study without having secondary IOP-lowering surgery in the study eye(s).

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
250 (estimated)
First submitted
29 Dec 2025
Start date
15 Sept 2025
Primary completion date
31 Dec 2030
Lead sponsor
Iantrek, Inc.
Diseases
Glaucoma
NCT number
NCT07480343

What you commit to

  • Study type: Observational
  • Planned participants: 250
  • From 15 Sept 2025 to the primary completion date, 31 Dec 2030
  • 10 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Secondary surgical intervention for long-term IOP control in the study eye(s)

Other illness

  • Systemic disease that, in the opinion of the Investigator, would put participant's health at risk and/or prevent completion of required study visits

Other

  • Early termination from CREST

Who the study is looking for

  • Diagnosis of open-angle glaucoma (OAG) in the study eye(s), including pigmentary and pseudoexfoliative glaucoma, at the time of CREST enrollment
  • Completed participation in CREST
  • Provide signed written consent using the Institutional Review Board (IRB)/Ethics Committee (EC) approved study-specific informed consent form (ICF)
  • Ability, comprehension, and willingness to follow study instructions

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CREST-XT Site 07
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
CREST-XT Site 03
Coordinator of this site? Confirm its status
Cape CoralUnited StatesUnknown status
CREST-XT Site 12
Coordinator of this site? Confirm its status
Chevy ChaseUnited StatesUnknown status
CREST-XT Site 04
Coordinator of this site? Confirm its status
CrossvilleUnited StatesUnknown status
CREST-XT Site 10
Coordinator of this site? Confirm its status
DeLandUnited StatesUnknown status
CREST-XT Site 01
Coordinator of this site? Confirm its status
Fort WashingtonUnited StatesUnknown status
CREST-XT Site 16
Coordinator of this site? Confirm its status
Las VegasUnited StatesUnknown status
CREST-XT Site 05
Coordinator of this site? Confirm its status
Newport BeachUnited StatesUnknown status
CREST-XT Site 13
Coordinator of this site? Confirm its status
RockvilleUnited StatesUnknown status
CREST-XT Site 11
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.