Changeflow GovPing Healthcare & Life Sciences Partial Ciliary Block Risk Study After Cataract...
Routine Notice Added Final

Partial Ciliary Block Risk Study After Cataract Surgery

Favicon for changeflow.com ClinicalTrials.gov Studies
Detected
Email

Summary

A prospective observational study (NCT07549438) will examine risk factors for developing classic or partial ciliary block following combined cataract surgery and goniosynechialysis in patients with primary angle-closure disease. Researchers will use non-invasive imaging modalities including ultrasound biomicroscopy and optical coherence tomography to measure anterior chamber width, lens thickness, and axial length before surgery, excluding patients with eye length under 19mm. Participants will undergo standard surgery and be monitored for 12 months during routine follow-up visits.

Published by NIH on changeflow.com . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

About this source

ClinicalTrials.gov is the NIH-run registry of every clinical trial conducted in the United States, plus most international trials sponsored by US-based companies or institutions. By federal law, sponsors must register Phase 2 through Phase 4 studies before enrolling patients and post results within a year of completion. This feed tracks every new trial registration and study update, around 700 a month: drug interventions, device studies, behavioral protocols, observational research. Watch this if you scout drug candidates moving into mid or late-stage development, monitor competitor pipelines, or follow rare disease research where new trials signal patient hope. GovPing parses sponsor, phase, intervention, and target indication on each entry.

What changed

The study registered on ClinicalTrials.gov describes a prospective, observational investigation examining risk predictors for ciliary block and aqueous misdirection following combined cataract extraction with goniosynechialysis in primary angle-closure disease patients. Researchers will employ standard imaging tools—ultrasound biomicroscopy and optical coherence tomography—to obtain detailed pre-surgical measurements of anterior segment structures. Patients with highly short axial length below 19mm are excluded from participation. As an observational study, participants will receive their scheduled standard-of-care surgery and be followed for 12 months.

For clinical investigators, ophthalmic surgeons, and healthcare facilities treating primary angle-closure glaucoma, this study may inform future pre-surgical risk stratification protocols. The exclusion criterion of axial length below 19mm reflects existing clinical awareness that very short eyes carry disproportionate risk. Institutions conducting similar angle-closure surgeries should monitor for emerging findings that could influence informed consent discussions or surgical planning.

Archived snapshot

Apr 24, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

Predicting the Risk of Partial Ciliary Block After Cataract and Goniosynechialysis Surgery in Primary Angle-Closure Disease

Observational NCT07549438 Kind: OBSERVATIONAL Apr 24, 2026

Abstract

Primary angle-closure disease (PACD) is a major cause of vision loss, often treated with a combined surgery that removes the eye's natural lens (cataract surgery) and physically opens the eye's drainage system (goniosynechialysis). While effective, this surgery carries a small risk of a severe complication called ciliary block (or aqueous misdirection), where fluid builds up in the wrong part of the eye, pushing structures forward and causing high eye pressure. Recently, doctors have also noticed a "partial" form of this block, which can slowly cause the eye's drainage angle to close again without immediate severe symptoms.

The purpose of this prospective, observational study is to identify which patients are at the highest risk for developing classic or partial ciliary block after this combined surgery. Researchers will use standard, non-invasive eye imaging tools-such as ultrasound biomicroscopy (UBM) and optical coherence tomography (OCT)-to take highly detailed measurements of the front of the eye before surgery. They will specifically look at factors like the width of the anterior chamber, the thickness of the lens, and the eye's overall length. To ensure accuracy, patients with a very short eye length (less than 19mm) will not be included in the study.

Because this is an observational study, participation will not change a patient's standard surgical plan. Patients will undergo their scheduled surgery and be monitored for 12 months during routine follow-up visits t...

Conditions: Primary Angle-Closure Glaucoma

View original document →

Get daily alerts for ClinicalTrials.gov Studies

Daily digest delivered to your inbox.

Free. Unsubscribe anytime.

About this page

What is GovPing?

Every important government, regulator, and court update from around the world. One place. Real-time. Free. Our mission

What's from the agency?

Source document text, dates, docket IDs, and authority are extracted directly from NIH.

What's AI-generated?

The summary, classification, recommended actions, deadlines, and penalty information are AI-generated from the original text and may contain errors. Always verify against the source document.

Last updated

Classification

Agency
NIH
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Healthcare providers Clinical investigators
Industry sector
6211 Healthcare Providers
Activity scope
Clinical research Patient monitoring Surgical outcomes
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Compliance frameworks
GxP
Topics
Medical Devices Public Health

Get alerts for this source

We'll email you when ClinicalTrials.gov Studies publishes new changes.

Free. Unsubscribe anytime.

You're subscribed!