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NCT07427160Recruiting

Prognostic Role of Macular Neovascular Membrane Subtype in Pneumatic Displacement of Macular Hemorrhages

Source: ClinicalTrials.gov · Last updated 23 Feb 2026

Brief summary (registry, in English)

This study investigates the prognostic value of macular neovascularization (MNV) subtypes in patients treated with pneumatic displacement for submacular hemorrhage. The researchers will compare anatomical and functional outcomes (visual acuity) between PCV, RAP, and other MNV forms within a Caucasian cohort to identify subtype-specific predictors of recovery.

Status (registry)
Recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
17 Feb 2026
Start date
15 Oct 2025
Primary completion date
15 Oct 2026
Lead sponsor
Marco Mazzola
NCT number
NCT07427160

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 15 Oct 2025 to the primary completion date, 15 Oct 2026
  • 1 site 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

  • Previous pneumatic displacement procedures for SMH in the study eye
  • Ocular surgery in the 8 weeks preceding the pneumatic displacement intervention

Other illness

  • SMH secondary to conditions other than MNV

Other

  • SMH estimated to be present for more than 15 days at the time of diagnosis
  • Presence of proliferative diabetic retinopathy in the study eye
  • Aphakia in the study eye
  • Inadequate pupillary dilation, media opacities, or other impediments to retinal imaging
  • Follow-up duration of less than 6 months following the procedure

Who the study is looking for

  • Patients undergoing pneumatic displacement (PD) for submacular hemorrhage (SMH), secondary to macular neovascularization (MNV)
  • Age 50 years or older at the time of SMH diagnosis
  • Caucasian ethnicity
  • SMH involving the central or internal ring of the Early Treatment Diabetic Retinopathy Study (ETDRS) grid (within a 3 mm circumference centered on the fovea)
  • SMH dimensions equal to or greater than one papillary diameter
  • Pneumatic displacement treatment performed within 36 hours of SMH diagnosis

Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Ospedale Santa Chiara di Trento
Coordinator of this site? Confirm its status
TrentoItalyRecruiting

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