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Trial · NCT07913412

High-precision Radiosurgery Followed by Minimally Invasive Surgical Approach in Patients With High-prominence Uveal Melanoma: Modern Radiation Techniques and Outcomes

NCT07913412, Recruiting, University Hospital, Essen

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. High-precision Radiosurgery Followed by Minimally Invasive Surgical Approach in Patients With High-prominence Uveal Melanoma: Modern Radiation Techniques and Outcomes. Trials, record NCT07913412. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07913412

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
High-precision Radiosurgery Followed by Minimally Invasive Surgical Approach in Patients With High-prominence Uveal Melanoma: Modern Radiation Techniques and Outcomes
NCT number
NCT07913412
Status
Recruiting
Enrollment
250 participants, estimated
Lead sponsor
University Hospital, Essen
Conditions
Uveal Melanoma, High-risk Uveal Melanoma, Prominent Uveal Melanoma
First posted
2026-11-03
Last updated
2026-11-03

Source ClinicalTrials.gov

Registered outcomes12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryLocal controlAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.Local control
PrimaryFunction: Visual acuity:At 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.Visual function assessed separately for each eye. Visual acuity: decimal scale,range 2,0 - 0,01: decimal acuity scale
PrimaryQuality of Life, ophthalmic cancer-specific quality of lifeAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.
Quality of Life, ophthalmic cancer-specific quality of life 1\) EORTC QLQ-OPT30 (ophthalmic cancer-specific quality of life): Scores range from 0-100; higher scores indicate greater visual impairment, ocular symptoms, and functional difficulties.
PrimaryProgression Free SurvivalAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.Progression Free Survival
PrimaryOverall SurvivalAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.Overall Survival
PrimaryFunction: Visual acuity:At 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.
Visual function assessed separately for each eye. Visual acuity: decimal scale,range 2,0 - 0,01: decimal acuity scale; furthermore, 1.Count-fingers, 2.hand-motion and 3.light-perception categories are recorded separately when acuity cannot be quantified: for each item: value yes / no
PrimaryFunction: Visual fieldAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.Visual field: Automated perimetry, Visual Field Index (VFI, %): 0 % - 100%,
PrimaryQuality of Life general quality of lifeAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.
EORTC QLQ-C30 (general quality of life): Scores range from 0-100; A) higher scores indicate better functioning/global quality of life B) symptom scores: indicate greater symptom burden on symptom scales.
PrimaryFunction: Retinal Nerve Fiber LayerAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.Optical coherence tomography (OCT): Peripapillary retinal nerve fiber layer (RNFL) thickness, measured in µm and classified in percentiles (regarding normal values)
PrimaryCorneaAt 3 months, every 6 months up to 24 months, and annually thereafter up to 60 -120 months.corneal outcome: thickness measured in µm

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
36230660BACKGROUND

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07913412

GET https://conductscience.org/api/trials/v1/NCT07913412/registered