Primary Completion Date
primary_completion_date
Optional
Date of final data collection for the primary outcome measure.
Clinical Trials API - ClinicalTrials.gov Search & Data Export
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from $2.10 / 1,000 results
Search ClinicalTrials.gov by condition, intervention, sponsor or status and pull clinical trial data into flat rows: NCT ID, status, phase, enrollment, sponsor, dates and locations. Ready for CSV, JSON or AI agent workflows, with no API key.
NCT ID
nct_id
Optional
Unique ClinicalTrials.gov study identifier, the primary key for this record.
Title
title
Optional
Brief public title of the study.
Official Title
official_title
Optional
Full official protocol title as registered.
Acronym
acronym
Optional
Short study acronym the sponsor uses in publications, when one is registered.
Sponsor Protocol ID
org_study_id
Optional
The sponsor's own internal protocol number for this study.
Secondary IDs
secondary_ids
Optional
Other registry, grant or regulatory identifiers for this study, comma separated (NIH grant numbers, EudraCT, WHO registry IDs).
Registering Organization
organization
Optional
Organization that submitted the record to ClinicalTrials.gov.
Organization Class
organization_class
Optional
Sector of the registering organization, for example INDUSTRY, NIH, OTHER_GOV or OTHER.
Source record URL
url
Optional
Canonical public ClinicalTrials.gov page for this study.
Overall Status
status
Optional
Current recruitment status of the study, for example RECRUITING or COMPLETED.
Last Known Status
last_known_status
Optional
Last status recorded before the study became UNKNOWN because the sponsor stopped updating it.
Why Stopped
why_stopped
Optional
Sponsor's stated reason the study was terminated, suspended or withdrawn.
Status Verified Date
status_verified_date
Optional
Month the sponsor last verified the study status, the best available freshness signal.
Start Date
start_date
Optional
Date the study started.
Start Date Type
start_date_type
Optional
Whether the start date is ACTUAL or still ESTIMATED.
Primary Completion Date
primary_completion_date
Optional
Date of final data collection for the primary outcome measure.
Primary Completion Date Type
primary_completion_date_type
Optional
Whether the primary completion date is ACTUAL or ESTIMATED.
Completion Date
completion_date
Optional
Date the study as a whole ended or is expected to end.
Completion Date Type
completion_date_type
Optional
Whether the completion date is ACTUAL or ESTIMATED.
First Posted Date
study_first_post_date
Optional
Date the study record was first posted publicly.
Results First Posted Date
results_first_post_date
Optional
Date summary results were first posted, empty when no results are posted.
Last Update Posted
last_update
Optional
Date the most recent update to this record was posted.
Has Expanded Access
has_expanded_access
Optional
Whether the sponsor offers expanded access to the intervention outside the trial.
Lead Sponsor
sponsor
Optional
Organization responsible for the overall conduct of the study.
Sponsor Class
sponsor_class
Optional
Sector of the lead sponsor, for example INDUSTRY, NIH, OTHER_GOV or OTHER.
Collaborators
collaborators
Optional
Other organizations collaborating on the study, comma separated.
Responsible Party Type
responsible_party_type
Optional
Who is accountable for the record, for example SPONSOR or PRINCIPAL_INVESTIGATOR.
Responsible Investigator
responsible_party_investigator
Optional
Name of the investigator named as responsible party.
Responsible Investigator Title
responsible_party_title
Optional
Job title of the responsible investigator.
Responsible Investigator Affiliation
responsible_party_affiliation
Optional
Institution the responsible investigator is affiliated with.
Has Data Monitoring Committee
oversight_has_dmc
Optional
Whether the study has an independent data monitoring committee.
FDA Regulated Drug
is_fda_regulated_drug
Optional
Whether the study involves an FDA-regulated drug or biologic product.
FDA Regulated Device
is_fda_regulated_device
Optional
Whether the study involves an FDA-regulated device product.
Conditions
conditions
Optional
Diseases or conditions studied, as written by the sponsor, comma separated.
Keywords
keywords
Optional
Sponsor-supplied search keywords for the study, comma separated.
MeSH Conditions
mesh_conditions
Optional
Normalized MeSH condition terms derived by ClinicalTrials.gov, comma separated. Use these instead of the free-text conditions when grouping studies.
Interventions
interventions
Optional
Names of the interventions being tested, comma separated.
Intervention Types
intervention_types
Optional
Distinct intervention categories used in the study, for example DRUG, DEVICE or BEHAVIORAL.
Intervention Other Names
intervention_other_names
Optional
Brand names, code names and synonyms for the interventions, comma separated.
MeSH Interventions
mesh_interventions
Optional
Normalized MeSH intervention or drug terms derived by ClinicalTrials.gov, comma separated.
Phase
phase
Optional
Trial phase or phases, for example PHASE2 or PHASE2, PHASE3. NA means a trial without FDA-defined phases.
Study Type
study_type
Optional
Study design category, for example INTERVENTIONAL, OBSERVATIONAL or EXPANDED_ACCESS.
Enrollment
enrollment
Optional
Number of participants enrolled or targeted.
Enrollment Type
enrollment_type
Optional
Whether the enrollment number is ACTUAL or still ESTIMATED.
Allocation
allocation
Optional
How participants are assigned to arms, RANDOMIZED or NON_RANDOMIZED.
Intervention Model
intervention_model
Optional
Trial arm structure, for example PARALLEL, CROSSOVER or SINGLE_GROUP.
Primary Purpose
primary_purpose
Optional
Main objective of the study, for example TREATMENT, PREVENTION or DIAGNOSTIC.
Masking
masking
Optional
Level of blinding, for example NONE, SINGLE, DOUBLE, TRIPLE or QUADRUPLE.
Who Masked
who_masked
Optional
Parties blinded to assignment, for example PARTICIPANT, INVESTIGATOR, OUTCOMES_ASSESSOR.
Observational Model
observational_model
Optional
Design of an observational study, for example COHORT or CASE_CONTROL.
Time Perspective
time_perspective
Optional
Time direction of an observational study, for example PROSPECTIVE or RETROSPECTIVE.
Arm Count
arm_count
Optional
Number of study arms or groups defined in the protocol.
Arm Groups
arm_groups
Optional
Labels of the study arms or groups, comma separated.
Primary Outcomes
primary_outcomes
Optional
Primary outcome measures, comma separated.
Primary Outcome Timeframe
primary_outcome_timeframe
Optional
Time frame over which the first primary outcome is measured.
Secondary Outcomes
secondary_outcomes
Optional
Secondary outcome measures, comma separated.
Minimum Age
min_age
Optional
Youngest age eligible for the study.
Maximum Age
max_age
Optional
Oldest age eligible for the study.
Standard Age Groups
std_ages
Optional
Standardized age brackets the study accepts: CHILD, ADULT, OLDER_ADULT.
Sex
sex
Optional
Sex eligible for the study: ALL, FEMALE or MALE.
Accepts Healthy Volunteers
healthy_volunteers
Optional
Whether the study accepts healthy volunteers.
Sampling Method
sampling_method
Optional
Sampling approach in an observational study, PROBABILITY_SAMPLE or NON_PROBABILITY_SAMPLE.
Study Population
study_population
Optional
Description of the population an observational study draws from.
Eligibility Criteria
eligibility_criteria
Optional
Full inclusion and exclusion criteria text, truncated to 5000 characters.
Location Count
location_count
Optional
Number of study sites listed on the record.
Recruiting Location Count
recruiting_location_count
Optional
Number of sites whose own record is marked RECRUITING. Empty when the source publishes no per-site status.
Countries
countries
Optional
Distinct countries with a study site, comma separated.
States
states
Optional
Distinct states or provinces with a study site, comma separated.
Cities
cities
Optional
Distinct cities with a study site, comma separated.
Locations
locations
Optional
Study sites as facility, city, state, country, comma separated and capped at 25 sites.
First Location Latitude
first_location_lat
Optional
Latitude of the first study site that has coordinates.
First Location Longitude
first_location_lon
Optional
Longitude of the first study site that has coordinates.
Central Contact Name
central_contact_name
Optional
Name of the central study contact for enrollment enquiries.
Central Contact Email
central_contact_email
Optional
Email address of the central study contact.
Central Contact Phone
central_contact_phone
Optional
Phone number of the central study contact.
Overall Official Name
overall_official_name
Optional
Name of the principal investigator or study director.
Overall Official Role
overall_official_role
Optional
Role of the overall official, for example PRINCIPAL_INVESTIGATOR or STUDY_DIRECTOR.
Overall Official Affiliation
overall_official_affiliation
Optional
Institution the overall official is affiliated with.
Brief Summary
brief_summary
Optional
Plain-language summary of the study, truncated to 2000 characters.
Detailed Description
detailed_description
Optional
Extended technical description of the study, truncated to 5000 characters.
PubMed IDs
pmids
Optional
PubMed IDs of publications linked to this study, comma separated.
IPD Sharing
ipd_sharing
Optional
Whether individual participant data will be shared: YES, NO or UNDECIDED.
Posted Document Types
document_types
Optional
Types of full documents posted with the record, for example Prot_SAP or ICF.
Has Results
has_results
Optional
Whether summary results have been posted for this study.
Serious Adverse Event Terms
serious_adverse_event_count
Optional
Number of distinct serious adverse event terms in the posted results. Empty when no results are posted.
Other Adverse Event Terms
other_adverse_event_count
Optional
Number of distinct non-serious adverse event terms in the posted results. Empty when no results are posted.
Data Version Date
version_date
Optional
Date of the ClinicalTrials.gov data snapshot this record came from.