RECRUITING

Ketorolac Levels in Vitreous and Aqueous Samples From Patients Undergoing Combined Cataract and Pars Plana Vitrectomy Surgeries With and Without Intracameral Phenylephrine 1.0% / Ketorolac 0.3%

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a clinical trial evaluating Ketorolac levels in vitreous and aqueous humor samples from patients undergoing combined cataract and pars plana vitrectomy surgeries with and without intracameral phenylephrine 1.0% / ketorolac 0.3% (OMIDRIA). Patients not receiving intracameral OMIDRIA will receive topical ketorolac prior to cataract surgery/pars plana vitrectomy.

Official Title

Ketorolac Levels in Vitreous and Aqueous Samples From Patients Undergoing Combined Cataract and Pars Plana Vitrectomy Surgeries With and Without Intracameral Phenylephrine 1.0% / Ketorolac 0.3%

Quick Facts

Study Start:2023-09-01
Study Completion:2026-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06539637

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Able to provide informed consent
  2. 2. Undergoing cataract surgery immediately followed by pars plana vitrectomy
  3. 3. Diagnosed preoperatively with a structural pathology requiring vitrectomy (e.g., epiretinal membrane, macular hole, and symptomatic vitreous floaters)
  4. 4. Willing and able to comply with all study procedures
  5. 5. Male or female, aged ≥ 18 years
  1. 1. Age \< 18
  2. 2. Participating in another clinical trial
  3. 3. Patients undergoing cataract surgery or pars plana vitrectomy alone (not a combined procedure)
  4. 4. Previous vitrectomy
  5. 5. Complications at the time of cataract surgery
  6. 6. A tear in the posterior capsule

Contacts and Locations

Study Contact

Eric Donnenfeld, MD
CONTACT
516 804 5200
ericdonnenfeld@gmail.com

Principal Investigator

Eric Donnenfeld, MD
PRINCIPAL_INVESTIGATOR
Ophthalmic Consultants of Long Island

Study Locations (Sites)

Ophthalmic Consultants of Long Island
Westbury, New York, 11590
United States

Collaborators and Investigators

Sponsor: DHS Consulting

  • Eric Donnenfeld, MD, PRINCIPAL_INVESTIGATOR, Ophthalmic Consultants of Long Island

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-09-01
Study Completion Date2026-02

Study Record Updates

Study Start Date2023-09-01
Study Completion Date2026-02

Terms related to this study

Additional Relevant MeSH Terms

  • Cataract