{"type":"trials","record":{"id":41910,"source_id":"clinicaltrials-gov","external_id":"NCT05686421","title":"Comfortable and Stabilizing Chin & Forehead Rest Attachment for Slit Lamp Configurations","brief_summary":"In this study, participants will be imaged using two Optical Coherence Tomography (OCT) devices: device N, a standard conventional OCT device with an invention (comfortable chin and forehead rest that can be adjusted to fit each individual's size) attached to the device; and device C, the standard conventional OCT device with no invention attached. The investigators will assess whether the chin and forehead rest attachment (invention) provides a more comfortable experience for patients.","overall_status":"Terminated","phases":[],"study_type":"INTERVENTIONAL","sponsor":"NYU Langone Health","enrollment":42,"countries":["United States"],"start_date":"2023-03-30","completion_date":"2023-04-28","last_update_date":"2024-11-05","source_url":"https://clinicaltrials.gov/study/NCT05686421","editorial_summary":"A registered study indexed because it matched monitored longevity research terms. Registry status: Terminated. Registration does not establish safety or effectiveness.","first_seen_at":"2026-09-25T01:25:30.378222+00:00","last_seen_at":"2026-09-25T06:20:47.789+00:00","metadata":{"sex":"ALL","acronym":null,"age_range":"18 Years","comparator":null,"organization":"NYU Langone Health","interventions":["OCT Imaging Using Device N","OCT Imaging Using Device C"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Percentage of Participants Who Indicate Device N Provided a More Comfortable Experience, Compared With Device C — Post-…","Comfort Level Rating of Device N on 0-5 Scale — Post-Imaging Session (Day 1)","Comfort Level Rating of Device C on 0-5 Scale — Post-Imaging Session (Day 1)","Time Duration to Adjust for Number of Motion Artifacts Present With Device N Imaging — Imaging Session (Day 1)","Time Duration to Adjust for Number of Motion Artifacts Present With Device C Imaging — Imaging Session (Day 1)"],"design_description":"RANDOMIZED · CROSSOVER · SUPPORTIVE CARE · DOUBLE","source_has_results":true},"controlled_terms":["Age-Related Macular Degeneration","Diabetic Retinopathy","Central Serous Chorioretinopathy","Glaucoma","Glaucoma, Suspect","Eye Diseases","OCT Imaging Using Device N","OCT Imaging Using Device C"],"relevance_confidence":60,"source_quality_score":100,"freshness_score":65,"publication_state":"published","match_explanation":"Source terminology contains: age-related macular degeneration.","quality_checked_at":"2026-09-25T06:20:59.355028+00:00","duplicate_cluster_key":"id:nct05686421","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2023-03-30 to 2023-04-28","comparator":null,"confidence":"structured-source","population":"ALL · 18 Years","provenance":{"duration":"start_date and completion_date","comparator":"registry arm fields","population":"registry eligibility fields","intervention":"registry intervention fields","participants":"enrollment","study_design":"study_type and registry design fields","evidence_stage":"phases","reported_outcome":"not available","outcomes_measured":"registry outcome-measure fields"},"generated_at":"2026-09-25T06:20:47.890Z","intervention":["OCT Imaging Using Device N","OCT Imaging Using Device C"],"participants":42,"study_design":"RANDOMIZED · CROSSOVER · SUPPORTIVE CARE · DOUBLE","subject_scope":"Human clinical study registration","evidence_stage":"Phase not reported","safety_context":"Eligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians.","source_support":"Structured registry protocol metadata; no finding-level conclusion is generated.","main_limitation":"This is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.","reported_outcome":null,"outcomes_measured":["Percentage of Participants Who Indicate Device N Provided a More Comfortable Experience, Compared With Device C — Post-…","Comfort Level Rating of Device N on 0-5 Scale — Post-Imaging Session (Day 1)","Comfort Level Rating of Device C on 0-5 Scale — Post-Imaging Session (Day 1)","Time Duration to Adjust for Number of Motion Artifacts Present With Device N Imaging — Imaging Session (Day 1)","Time Duration to Adjust for Number of Motion Artifacts Present With Device C Imaging — Imaging Session (Day 1)"],"regulatory_context":"Trial registration is not regulatory approval and does not establish that an intervention is available."},"clinical_trial_topics":[{"topic_slug":"vision-aging","is_published":true,"match_reasons":["Source terminology contains: age-related macular degeneration.","Source terminology supplies longevity context: aging, age-related.","Study type is explicitly identified as INTERVENTIONAL."],"matched_fields":["controlled terminology","controlled context","study type"],"relevance_score":60,"intelligence_topics":{"name":"Vision ageing","slug":"vision-aging"}}],"content_sources":{"name":"ClinicalTrials.gov","homepage_url":"https://clinicaltrials.gov/"}},"canonical_url":"https://www.immortal.life/trials/41910","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}