NCT06617273

Brief Summary

Diabetes mellitus is a chronic metabolic disease that can lead to visual impairment and eye complications such as diabetic retinopathy and diabetic macular edema. Diabetics are considered a vulnerable patient group for cataract surgery, as microincision phacoemulsification (MICS) in diabetics is associated with a higher risk of postoperative swelling of the macula and cornea (macular or corneal edema). In addition, the ultrasound energy emitted during MICS, high and fluctuating intraocular pressure and the movement of surgical instruments and lens material are the main causes of surgical trauma. The medical device "Centurion Vision System" with the "Active Sentry" handpiece was developed specifically to improve the stability of the anterior chamber during surgery and to enable operations at low, almost normal physiological intraocular pressure settings. The central question of the study is therefore, whether a stable intraocular pressure close to physiological normal conditions (28 mmHg) during surgery can lead to a reduction in surgical trauma. In this prospective and randomized study, patients suffering from diabetes and having a planned bilateral MICS are included in one of two study arms: A) The participant is operated on with an IOP of 28 mm Hg in the better eye and an IOP of 50 mm Hg in the worse eye or B) the participant is operated on with an IOP of 28 mm Hg in the worse eye and an IOP of 50 mm Hg in the better eye.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2024

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

August 21, 2024

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

September 11, 2024

Completed
16 days until next milestone

First Posted

Study publicly available on registry

September 27, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2025

Completed
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2025

Completed
Last Updated

September 27, 2024

Status Verified

September 1, 2024

Enrollment Period

1 year

First QC Date

September 11, 2024

Last Update Submit

September 24, 2024

Conditions

Keywords

Diabetic RetinopathyPhacoemulsificationMicroincision PhacoemulsificationCataractIntraocular pressureActive anterior chamber pressure

Outcome Measures

Primary Outcomes (1)

  • Delta ACF

    Difference from pre- to postoperative ACF (delta ACF) at day 1 (FU1) and day 7 (FU2) after cataract surgery.

    1 week

Secondary Outcomes (12)

  • BCVA

    1 month

  • 5mm corneal volume

    1 month

  • Anterior chamber depth

    1 month

  • Mydriatic pupil width

    1 month

  • Endothelial cell density

    1 month

  • +7 more secondary outcomes

Study Arms (2)

A) IOP 28mmHg on the better eye and IOP 50mmHg on the worse eye

OTHER

Near normal intraocular pressure cataract surgery using active anterior chamber pressure sensing and regulation

Device: Ophthalmosurgical handpiece with active anterior chamber pressure sensing and regulation

B) IOP 28mmHg on worse eye and IOP 50mmHg on the better eye

OTHER

Near normal intraocular pressure cataract surgery using active anterior chamber pressure sensing and regulation

Device: Ophthalmosurgical handpiece with active anterior chamber pressure sensing and regulation

Interventions

Cataract surgery in patients with diabetic retinopathy using active anterior chamber pressure sensing and regulation

A) IOP 28mmHg on the better eye and IOP 50mmHg on the worse eyeB) IOP 28mmHg on worse eye and IOP 50mmHg on the better eye

Eligibility Criteria

Age50 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Indication for immediate sequential bilateral microincision cataract surgery
  • Diagnosis of Diabetes Mellitus treated with oral medication or insulin therapy and confirmed by HbA1c ≥6,5 %
  • Presence of diabetic retinopathy grade ≥1 on the international clinical diabetic retinopathy (ICDR) severity scale
  • LOCS 2-4 with no more than 1 grade difference between both eyes
  • Male or female patient aged 50 - 85 years of age at time of consent
  • Understands and agrees to comply with the study procedures and provides written informed consent as documented by signature

You may not qualify if:

  • Participation in another clinical trial within 30 days before pre-screening and throughout the trial
  • Prior intraocular surgery of any type
  • History of diabetic macular edema
  • Presence of macular edema, defined as central retinal thickness of \>300 µm plus intraretinal or subretinal fluid on OCT within range of 1mm of foveal center
  • Presence of any retinal or choroidal disease, other than diabetes, that could affect retinal thickness
  • Known history of uveitis
  • Documented use of systemic or topical steroid or other immunosuppressive medication within the last 3 months
  • ACF \>10 ph/ms. ACF difference between right and left eye \> 4ph/ms
  • Difference of DRP grading between right and left eye of more than 1 grade (ICDR)
  • Inability to measure total macular volume due to, but not limed to, too dense cataract, vitreous bleeding
  • Woman of childbearing potential (WOCBP) who is breastfeeding, has a positive urine pregnancy test, is not willing to undergo a urine pregnancy test upon entering or exiting the study, intends to become pregnant during the study, or does not agree to use adequate birth control methods for the duration of the study
  • Patients in possession of an active implantable medical device (AIMD)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medical University Innsbruck, University Hospital for Ophthalmology and Optometry

Innsbruck, 6020, Austria

Location

MeSH Terms

Conditions

Diabetic RetinopathyCataract

Condition Hierarchy (Ancestors)

Retinal DiseasesEye DiseasesDiabetic AngiopathiesVascular DiseasesCardiovascular DiseasesDiabetes ComplicationsDiabetes MellitusEndocrine System DiseasesLens Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: controlled randomized, comparative
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 11, 2024

First Posted

September 27, 2024

Study Start

August 21, 2024

Primary Completion

September 1, 2025

Study Completion

September 30, 2025

Last Updated

September 27, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

Locations