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Enrolling by invitationNCT07682025Updated Jul 2, 2026

Imaging and Predictive Modelling of Proliferative Vitreoretinopathy.

An observational study in Proliferative Vitreoretinopathy, sponsored by University College, London. Enrolling by invitation at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-02.

Sponsored by University College, London · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

Patients with retinal detachment are at risk of recurrence and failure of surgery requiring multiple surgeries due to a condition called proliferative vitreoretinopathy (PVR).

Study aims to help tailor patients' treatments and improve outcomes by:

[i] studying imaging biomarkers of PVR, and [ii] develop AI models for PVR detection.

Inclusion:

  • Patients with 'complicated' retinal detachment with PVR recruited to a phase 1 dose-finding trial called MORPH-1.
  • Patients with 'simple' retinal detachment without PVR recruited to a PhD study.

Non -invasive multimodal imaging and anonymized imaging will be used to study imaging biomarkers of PVR and develop deep learning models to predict PVR in collaboration with an artificial intelligence (AI) expert team at UCL Institute of Ophthalmology.

02

Conditions studied

  • Proliferative Vitreoretinopathy
03

In context

Vitreoretinopathy, Proliferative

35 studies on the registry are indexed under Vitreoretinopathy, Proliferative; 9 are open to participants now.

Browse Vitreoretinopathy, Proliferative studies →

Lead sponsor

University College, London is the lead sponsor of 632 studies on the registry; 145 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

MORPH-1 - PVR detachments Cohort-NHS - primary RRD without PVR requiring PPV with PVD.

Inclusion criteria

  • MORPH-1 and Cohort-NHS study imaging

Exclusion criteria

Exclusion Criteria:

  • Participants from above studies who have not consented for image analysis and AI related analysis.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Target follow-up
3 Months
Patient registry
Yes

Groups and cohorts

  • Rhegmatogenous retinal detachment without proliferative vitreoretinopathy

    Rhegmatogenous retinal detachment without proliferative vitreoretinopathy at the time of their primary surgery

  • Rhegmatogenous retinal detachment with proliferative vitreoretinopathy

    Rhegmatogenous retinal detachment with proliferative vitreoretinopathy at the time of their primary surgery or post-operatively with recurrent retinal detachment.

06

What researchers measure

Primary outcomes

  1. To study multimodal imaging biomarkers of PVR.

    Use multimodal imaging namely widefield Optos, Widefield OCT, OCT macula, OCT disc, OCT EDI and OCTA to describe biomarkers of PVR.

    Time frame: Preoperative biomarkers of PVR on cases with established PVR Post-operative biomarkers of PVR on cases that develop PVR in the first 3 months.

Secondary outcomes

  1. To develop deep learning AI models for PVR detection in retinal detachment.

    Use widefield Optos imaging and OCT to: * Develop outputs for presence of PVR (binary), and * Develop output for prediction of PVR grade.

    Time frame: Post-operative 3 months

07

Study locations

1 site
  • University College London
    London, United Kingdom
08

References and documents

Individual participant data

Plan to share: No — Within participant's consent.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07682025
Lead sponsor
University College, London
Responsible party
Sponsor
First posted
Jul 2, 2026
Start date
Oct 12, 2026 (estimated)
Primary completion
Oct 15, 2027 (estimated)
Completion
Oct 15, 2027 (estimated)
Last update
Jul 2, 2026

Study contacts

James Bainbridge
principal investigator · University College, London

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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