primaryCompletionDate
Optional
Clinical Trials FDA Scraper
Pricing
Pay per usage
Extract clinical trials from ClinicalTrials.gov and FDA data from openFDA APIs. Search by condition, drug, sponsor, or NCT ID. Get adverse events, drug labels, recalls, and device data. For pharma research and regulatory monitoring.
dataType
Optional
Record discriminator: clinical_trial, drug_adverse_event, adverse_event_summary, drug_label, drug_recall, drug_approval, device_adverse_event, device_recall, device_510k, or run_status
dataSource
Optional
Origin of the record (e.g. ClinicalTrials.gov, openFDA FAERS, openFDA SPL)
apiVersion
Optional
Source API version (clinical trials only, 'v2')
scrapedAt
Optional
ISO 8601 timestamp when the record was extracted
nctId
Optional
orgStudyId
Optional
secondaryIds
Optional
briefTitle
Optional
officialTitle
Optional
acronym
Optional
url
Optional
overallStatus
Optional
startDate
Optional
startDateType
Optional
primaryCompletionDate
Optional
primaryCompletionDateType
Optional
completionDate
Optional
studyFirstPostDate
Optional
resultsFirstPostDate
Optional
lastUpdatePostDate
Optional
studyType
Optional
phases
Optional
designAllocation
Optional
designInterventionModel
Optional
designMasking
Optional
designPrimaryPurpose
Optional
enrollmentCount
Optional
enrollmentType
Optional
numberOfArms
Optional
eligibilityCriteria
Optional
sex
Optional
minimumAge
Optional
maximumAge
Optional
healthyVolunteers
Optional
conditions
Optional
keywords
Optional
interventions
Optional
Array of { type, name, description, armGroupLabels }
armGroups
Optional
Array of { label, type, description }
primaryOutcomes
Optional
Array of { measure, description, timeFrame }
secondaryOutcomes
Optional
Array of { measure, description, timeFrame }
leadSponsor
Optional
{ name, class }
collaborators
Optional
Array of { name, class }
locations
Optional
Array of { facility, city, state, country, status, geoPoint }
locationCount
Optional
countries
Optional
briefSummary
Optional
detailedDescription
Optional
isFDARegulatedDrug
Optional
isFDARegulatedDevice
Optional
hasExpandedAccess
Optional
aiSummary
Optional
Optional per-trial summary: { aiGenerated, summary, model?, generatedAt }
drugName
Optional
Drug queried for the adverse_event_summary record
aiGenerated
Optional
summary
Optional
model
Optional
eventCount
Optional
generatedAt
Optional
seriousCount
Optional
fatalCount
Optional
topReactions
Optional
Array of { reaction, count } (rule-based AE summary only)
safetyReportId
Optional
receiveDate
Optional
reportDate
Optional
reportType
Optional
serious
Optional
seriousnessDeath
Optional
seriousnessLifeThreatening
Optional
seriousnessHospitalization
Optional
seriousnessDisabling
Optional
seriousnessCongenitalAnomaly
Optional
seriousnessOther
Optional
patientAge
Optional
patientAgeUnit
Optional
patientSex
Optional
patientWeight
Optional
drugs
Optional
Adverse-event drugs: { name, brandName, genericName, manufacturerName, indication, route, dosageForm, activeSubstance, drugCharacterization }
reactions
Optional
Array of { reaction, outcome, outcomeLabel }
companynumb
Optional
occurCountry
Optional
primarySource
Optional
id
Optional
setId
Optional
version
Optional
effectiveTime
Optional
brandName
Optional
genericName
Optional
manufacturerName
Optional
productType
Optional
route
Optional
substanceName
Optional
pharmClassEpc
Optional
pharmClassMoa
Optional
rxcui
Optional
splId
Optional
unii
Optional
nui
Optional
indicationsAndUsage
Optional
dosageAndAdministration
Optional
contraindications
Optional
warningsAndCautions
Optional
boxedWarning
Optional
adverseReactions
Optional
drugInteractions
Optional
overdosage
Optional
pregnancy
Optional
nursingMothers
Optional
pediatricUse
Optional
geriatricUse
Optional
hasBoxedWarning
Optional
recallNumber
Optional
eventId
Optional
status
Optional
recallingFirm
Optional
city
Optional
state
Optional
country
Optional
voluntaryMandated
Optional
classification
Optional
classificationNumber
Optional
productDescription
Optional
codeInfo
Optional
productQuantity
Optional
reasonForRecall
Optional
recallInitiationDate
Optional
centerClassificationDate
Optional
terminationDate
Optional
distributionPattern
Optional
initialFirmNotification
Optional
applicationNumber
Optional
sponsorName
Optional
originalApprovalDate
Optional
products
Optional
Array of { productNumber, brandName, dosageForm, route, marketingStatus, teCode, activeIngredients:[{name,strength}] }
submissionCount
Optional
latestSubmission
Optional
{ type, number, status, statusDate } or null
reportNumber
Optional
eventType
Optional
dateReceived
Optional
dateReport
Optional
dateOfEvent
Optional
adverseEventFlag
Optional
productProblemFlag
Optional
eventDescription
Optional
manufacturerNarrative
Optional
devices
Optional
Device-event devices: { brandName, genericName, manufacturerName, modelNumber, catalogNumber, lotNumber, deviceOperator, implantFlag, dateRemoved }
deviceCount
Optional
patientSequence
Optional
reportSourceCode
Optional
reporterOccupation
Optional
healthProfessional
Optional
initialReportToFda
Optional
kNumber
Optional
applicant
Optional
contact
Optional
address
Optional
{ line1, line2, city, state, zip, country }
deviceName
Optional
productCode
Optional
regulatoryClass
Optional
decisionDate
Optional
decisionDescription
Optional
clearanceType
Optional
reviewAdviseCommittee
Optional
statementOrSummary
Optional
expeditedReviewFlag
Optional
thirdPartyFlag
Optional
message
Optional
Human-readable note (run_status record only)
dataSources
Optional
Data sources requested for the run (run_status record only)
stats
Optional
Per-type record counts for the run (run_status record only)