{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Hyperopia&page=2",
    "query": {
      "condition": "Hyperopia",
      "page": 2
    },
    "page_size": 10
  },
  "pagination": {
    "page": 2,
    "page_size": 10,
    "total_count": 10,
    "total_pages": 1,
    "next_page_url": null,
    "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Hyperopia&page=1&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-06-11T04:14:07.265Z",
  "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.",
  "notes": [
    "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.",
    "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.",
    "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees."
  ],
  "trials": [
    {
      "nct_id": "NCT06462456",
      "title": "Post-market Clinical Follow-up Study of Alcon PRECISION1™ Spherical and PRECISION1™ for Astigmatism Soft Contact Lenses",
      "overall_status": "TERMINATED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Refractive Errors"
      ],
      "interventions": [
        {
          "name": "Verofilcon A spherical soft contact lenses",
          "type": "DEVICE"
        },
        {
          "name": "Verofilcon A toric soft contact lenses",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Alcon Research",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "7 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "7 Years and older"
      },
      "enrollment_count": 140,
      "start_date": "2024-08-30",
      "completion_date": "2025-03-11",
      "has_results": false,
      "last_update_posted_date": "2025-07-20",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 12,
      "location_summary": "San Diego, California • Jacksonville, Florida • Orlando, Florida + 9 more",
      "locations": [
        {
          "city": "San Diego",
          "state": "California"
        },
        {
          "city": "Jacksonville",
          "state": "Florida"
        },
        {
          "city": "Orlando",
          "state": "Florida"
        },
        {
          "city": "Blue Island",
          "state": "Illinois"
        },
        {
          "city": "Chicago",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06462456"
    },
    {
      "nct_id": "NCT00762281",
      "title": "Safety and Effectiveness Study of the MEL 80 Excimer Laser Using LASIK in the Treatment of Hyperopia",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Hyperopia"
      ],
      "interventions": [
        {
          "name": "MEL 80 Hyperopic LASIK Treatment",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Carl Zeiss Meditec, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "21 Years and older"
      },
      "enrollment_count": 189,
      "start_date": "2004-07",
      "completion_date": "2008-10",
      "has_results": false,
      "last_update_posted_date": "2012-08-13",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 6,
      "location_summary": "San Diego, California • Greenwood Village, Colorado • Kansas City, Missouri + 3 more",
      "locations": [
        {
          "city": "San Diego",
          "state": "California"
        },
        {
          "city": "Greenwood Village",
          "state": "Colorado"
        },
        {
          "city": "Kansas City",
          "state": "Missouri"
        },
        {
          "city": "Eugene",
          "state": "Oregon"
        },
        {
          "city": "Austin",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00762281"
    },
    {
      "nct_id": "NCT03881670",
      "title": "On-Eye Optical Quality of Lotrafilcon B Lenses Over 12 Hours",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Hyperopia",
        "Myopia"
      ],
      "interventions": [
        {
          "name": "Lotrafilcon B",
          "type": "DEVICE"
        },
        {
          "name": "lotrafilcon B with Hydraluxe",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Indiana University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "35 Years",
        "sex": "ALL",
        "summary": "18 Years to 35 Years"
      },
      "enrollment_count": 24,
      "start_date": "2018-12-07",
      "completion_date": "2019-02-08",
      "has_results": true,
      "last_update_posted_date": "2020-03-10",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 1,
      "location_summary": "Bloomington, Indiana",
      "locations": [
        {
          "city": "Bloomington",
          "state": "Indiana"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03881670"
    },
    {
      "nct_id": "NCT03610997",
      "title": "Photorefractive Keratectomy for Severe Anisometropia and Isoametropia Associated With Amblyopia",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Anisometropia",
        "Hyperopia",
        "High Myopia",
        "Amblyopia Isometropic",
        "Amblyopia Bilateral",
        "High Astigmatism"
      ],
      "interventions": [
        {
          "name": "Photorefractive keratectomy",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Baylor College of Medicine",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "2 Years",
        "maximum_age": "17 Years",
        "sex": "ALL",
        "summary": "2 Years to 17 Years"
      },
      "enrollment_count": 200,
      "start_date": "2001-01-01",
      "completion_date": "2024-09-01",
      "has_results": false,
      "last_update_posted_date": "2025-12-08",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 1,
      "location_summary": "Houston, Texas",
      "locations": [
        {
          "city": "Houston",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03610997"
    },
    {
      "nct_id": "NCT04403542",
      "title": "Pilot Clinical Performance of a Silicone Hydrogel Lens for Up to Six Nights of Extended Wear",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Refractive Errors",
        "Myopia",
        "Hyperopia"
      ],
      "interventions": [
        {
          "name": "Lehfilcon A contact lens",
          "type": "DEVICE"
        },
        {
          "name": "Comfilcon A contact lens",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Alcon Research",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 36,
      "start_date": "2020-08-03",
      "completion_date": "2020-08-31",
      "has_results": true,
      "last_update_posted_date": "2023-08-22",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 3,
      "location_summary": "Medina, Minnesota • Granville, Ohio • Memphis, Tennessee",
      "locations": [
        {
          "city": "Medina",
          "state": "Minnesota"
        },
        {
          "city": "Granville",
          "state": "Ohio"
        },
        {
          "city": "Memphis",
          "state": "Tennessee"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04403542"
    },
    {
      "nct_id": "NCT03929588",
      "title": "Study of a Hand-held Device Plus Mobile App Versus Standard Eye Care Devices in Measuring Refractive Error of the Eye",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Refractive Errors",
        "Astigmatism"
      ],
      "interventions": [
        {
          "name": "Hand-held device supported by a mobile application",
          "type": "DEVICE"
        },
        {
          "name": "Phoropter",
          "type": "DEVICE"
        },
        {
          "name": "Autorefractor",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "EyeQue Corp.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "30 Years",
        "maximum_age": "65 Years",
        "sex": "ALL",
        "summary": "30 Years to 65 Years"
      },
      "enrollment_count": 230,
      "start_date": "2019-05-07",
      "completion_date": "2020-03-31",
      "has_results": true,
      "last_update_posted_date": "2022-03-24",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 1,
      "location_summary": "Inglewood, California",
      "locations": [
        {
          "city": "Inglewood",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03929588"
    },
    {
      "nct_id": "NCT04883996",
      "title": "A Phase 1/2 Crossover Study to Assess EXP039 for Myopia or Hyperopia",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1",
        "PHASE2"
      ],
      "conditions": [
        "Hyperopia",
        "Myopia"
      ],
      "interventions": [
        {
          "name": "1% EXP039",
          "type": "DRUG"
        },
        {
          "name": "Saline control",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "DRUG",
        "OTHER"
      ],
      "sponsor": "Canyon City Eyecare",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "80 Years",
        "sex": "ALL",
        "summary": "18 Years to 80 Years"
      },
      "enrollment_count": 60,
      "start_date": "2020-12-01",
      "completion_date": "2021-08-30",
      "has_results": false,
      "last_update_posted_date": "2021-05-13",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 1,
      "location_summary": "Azusa, California",
      "locations": [
        {
          "city": "Azusa",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04883996"
    },
    {
      "nct_id": "NCT05254587",
      "title": "Accuracy of IOLMASTER 700 Total Keratometry (TK)",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Myopia",
        "Hyperopia",
        "Cataract"
      ],
      "interventions": [
        {
          "name": "IOLMASTER 700 TK",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Advanced Vision Care",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 155,
      "start_date": "2022-02-08",
      "completion_date": "2024-01-27",
      "has_results": false,
      "last_update_posted_date": "2026-02-20",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 7,
      "location_summary": "Bakersfield, California • Los Angeles, California • Torrance, California + 4 more",
      "locations": [
        {
          "city": "Bakersfield",
          "state": "California"
        },
        {
          "city": "Los Angeles",
          "state": "California"
        },
        {
          "city": "Torrance",
          "state": "California"
        },
        {
          "city": "Bowie",
          "state": "Maryland"
        },
        {
          "city": "Bala-Cynwyd",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05254587"
    },
    {
      "nct_id": "NCT06098339",
      "title": "Performance Evaluation of Reusable Contact Lenses When Worn For One Month By Habitual Soft Contact Lens Wearers",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Myopia",
        "Hyperopia"
      ],
      "interventions": [
        {
          "name": "Lens A (fanfilcon A)",
          "type": "DEVICE"
        },
        {
          "name": "Lens B (lotrafilcon B)",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "CooperVision, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "39 Years",
        "sex": "ALL",
        "summary": "18 Years to 39 Years"
      },
      "enrollment_count": 53,
      "start_date": "2023-11-13",
      "completion_date": "2024-04-04",
      "has_results": true,
      "last_update_posted_date": "2024-08-28",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 2,
      "location_summary": "Ocoee, Florida • State College, Pennsylvania",
      "locations": [
        {
          "city": "Ocoee",
          "state": "Florida"
        },
        {
          "city": "State College",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06098339"
    },
    {
      "nct_id": "NCT03669146",
      "title": "Enhancement of Emmetropization in Highly Hyperopic Infants",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Hyperopia"
      ],
      "interventions": [
        {
          "name": "Glasses",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Donald O Mutti, OD, PhD",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "8 Weeks",
        "maximum_age": "15 Weeks",
        "sex": "ALL",
        "summary": "8 Weeks to 15 Weeks"
      },
      "enrollment_count": 35,
      "start_date": "2019-04-24",
      "completion_date": "2023-01-05",
      "has_results": true,
      "last_update_posted_date": "2024-07-09",
      "last_synced_at": "2026-06-11T04:14:07.265Z",
      "location_count": 1,
      "location_summary": "Columbus, Ohio",
      "locations": [
        {
          "city": "Columbus",
          "state": "Ohio"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03669146"
    }
  ]
}