{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=MAOA",
    "query": {
      "condition": "MAOA"
    },
    "page_size": 10
  },
  "pagination": {
    "page": 1,
    "page_size": 10,
    "total_count": 1,
    "total_pages": 1,
    "next_page_url": null,
    "previous_page_url": null
  },
  "source": "local",
  "last_synced_at": "2026-05-20T01:19:06.115Z",
  "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": "NCT01238250",
      "title": "Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight",
      "overall_status": "RECRUITING",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "15Q13.3 Deletion Syndrome",
        "15Q24 Deletion",
        "15q11.2 BP1-BP2 Deletion",
        "15q15 Deletions",
        "16P11.2 Deletion Syndrome",
        "16P12.2 Microdeletion",
        "16P13.11 Microdeletion Syndrome (Disorder)",
        "16p11.2 Duplications",
        "16p11.2 Triplications",
        "16p13.3 Deletion",
        "17Q11.2 Microduplication Syndrome (Disorder)",
        "17Q12 Duplication Syndrome",
        "17Q12 Microdeletion Syndrome (Disorder)",
        "17Q21.31 Deletion Syndrome",
        "17p13.3",
        "17q21.3 Duplications",
        "1Q21.1 Deletion",
        "1Q21.1 Microduplication Syndrome (Disorder)",
        "2Q37 Deletion Syndrome",
        "2p16.3 Deletions",
        "2q34 Duplication",
        "2q37.3 Deletion",
        "5P Deletion Syndrome",
        "5q35 Deletions",
        "5q35 Duplications",
        "6q16 Deletion",
        "7q11.23 Duplications",
        "9q34 Duplications",
        "ACTB",
        "ACTL6B",
        "ADNP",
        "ADSL",
        "AFF2",
        "AHDC1",
        "ALDH5A1",
        "ANK2",
        "ANK3",
        "ANKRD11",
        "ARHGEF9",
        "ARID1B",
        "ARX",
        "ASH1L",
        "ATRX Gene Mutation",
        "AUTS2 Syndrome",
        "BCKDK",
        "BCL11A",
        "BRSK2",
        "CACNA1C",
        "CAPRIN1",
        "CASK",
        "CASZ1",
        "CHAMP1",
        "CHD2",
        "CHD3",
        "CHD8",
        "CIC",
        "CLCN4",
        "CNOT3",
        "CREBBP Gene Mutation",
        "CSDE1",
        "CSNK2A1",
        "CSNK2B",
        "CTBP1",
        "CTCF",
        "CTNNB1 Gene Mutation",
        "CUL3",
        "DDX3X",
        "DEAF1",
        "DHCR7",
        "DLG4",
        "DNMT3A",
        "DSCAM",
        "DYNC1H1",
        "DYRK1A",
        "EBF3",
        "EHMT1",
        "EIF3F",
        "EP300 Gene Mutation",
        "FOXP1",
        "GIGYF1",
        "GNB1",
        "GRIN1",
        "GRIN2A",
        "GRIN2B",
        "GRIN2D",
        "HECW2",
        "HIVEP2-Related Intellectual Disability",
        "HNRNPC",
        "HNRNPD",
        "HNRNPH2",
        "HNRNPK",
        "HNRNPR",
        "HNRNPU",
        "HNRNPUL2",
        "IQSEC2-Related Syndromic Intellectual Disability",
        "IRF2BPL",
        "KANSL1",
        "KATNAL2",
        "KCNB1",
        "KDM3B",
        "KDM5B",
        "KDM6B",
        "KMT2A",
        "KMT2C Gene Mutation",
        "KMT2E",
        "KMT5B",
        "MAOA",
        "MAOB",
        "MBD5",
        "MBOAT7",
        "MED13",
        "MED13L",
        "MEF2C",
        "MEIS2",
        "MYT1L",
        "NAA15",
        "NBEA",
        "NCKAP1",
        "NEXMIF",
        "NIPBL",
        "NLGN2",
        "NLGN3",
        "NLGN4X",
        "NR3C2",
        "NR4A2",
        "NRXN1",
        "NRXN2",
        "NSD1 Gene Mutation",
        "PACS1",
        "PACS2",
        "PHF21A",
        "PHF3",
        "PHIP",
        "POMGNT1",
        "PPP2R1A",
        "PPP2R5D-Related Intellectual Disability",
        "PPP3CA",
        "PSMD12",
        "PTCHD1",
        "RALGAPB",
        "RELN",
        "RERE",
        "REST",
        "RFX3",
        "RIMS1",
        "RORB",
        "SCN1A",
        "SCN1B",
        "SCN2A Encephalopathy",
        "SETBP1 Gene Mutation",
        "SETD2 Gene Mutation",
        "SETD5",
        "SHANK2",
        "SIN3A",
        "SLC6A1",
        "SLC9A6",
        "SMARCA4 Gene Mutation",
        "SMARCC2",
        "SON",
        "SOX5",
        "SPAST",
        "SRCAP",
        "STXBP1 Encephalopathy With Epilepsy",
        "SYNCRIP",
        "SYNGAP1-Related Intellectual Disability",
        "TANC2",
        "TAOK1",
        "TBR1",
        "TCF20",
        "TCF7L2 Gene Mutation",
        "TLK2",
        "TRIO",
        "TRIP12",
        "UPF3B",
        "USP9X",
        "VPS13B",
        "WAC",
        "WDFY3",
        "Xp11.22 Duplication",
        "Xq28 Duplication",
        "YY1",
        "ZBTB20",
        "ZNF292",
        "ZNF462"
      ],
      "interventions": [],
      "intervention_types": [],
      "sponsor": "Simons Searchlight",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": null,
        "maximum_age": null,
        "sex": "ALL",
        "summary": "Not listed"
      },
      "enrollment_count": 100000,
      "start_date": "2010-10",
      "completion_date": "2050-10",
      "has_results": false,
      "last_update_posted_date": "2025-06-06",
      "last_synced_at": "2026-05-20T01:19:06.115Z",
      "location_count": 2,
      "location_summary": "Boston, Massachusetts • Lewisburg, Pennsylvania",
      "locations": [
        {
          "city": "Boston",
          "state": "Massachusetts"
        },
        {
          "city": "Lewisburg",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01238250"
    }
  ]
}