Tracka
For Research Institutions

Research-Grade SCD Data Without the Collection Burden

Access the largest structured sickle cell dataset in Africa through our enterprise API. Anonymized, ethics-compliant, and ready for analysis — no field work required.

The Challenge

Problems You Face Every Day

Traditional approaches to sickle cell tracking leave critical gaps that cost lives and waste resources.

Small Sample Sizes

Most SCD studies rely on single-facility cohorts of a few hundred patients, limiting statistical power and generalizability of findings.

Ethics & Consent Complexity

Obtaining individual consent for retrospective data analysis is costly and time-consuming, delaying research timelines by months.

Unstructured Data

Clinical data from partner facilities arrives in inconsistent formats — different coding systems, missing fields, and no standardized terminology.

The Solution

How Tracka Transforms Your Workflow

Purpose-built for sickle cell disease management with the tools your team actually needs.

Enterprise Data API

Query anonymized SCD data programmatically. Filter by genotype, region, age group, clinical domain, and more. Paginated responses with rate limiting.

Clinical-Grade Anonymization

All personally identifiable information is stripped using k-anonymity principles. Data is safe for IRB-exempt secondary analysis.

Cohort Building Tools

Define research cohorts using any combination of clinical, demographic, and geographic criteria. Export structured datasets in CSV or JSON.

Ethics-Ready Documentation

Every API response includes data provenance metadata. We provide template IRB applications and data use agreements for streamlined approval.

Longitudinal Data Access

Access multi-year patient trajectories including crisis frequency trends, medication adherence curves, and growth velocity data.

Multi-Center Coverage

Draw from 342+ facilities across 24 states. Your research benefits from geographic and demographic diversity that single-site studies cannot match.

Feature Highlights

Everything You Need, Nothing You Don't

  • RESTful API with comprehensive documentation, SDKs, and sandbox environment
  • Anonymized datasets covering 12,800+ patients across 342 facilities in 24 states
  • Cohort builder with filters for genotype, age, region, crisis frequency, and medication use
  • Longitudinal data spanning multiple years of clinical encounters per patient
  • Clinical-grade anonymization using k-anonymity — no PII in any API response
  • Data export in CSV, JSON, and FHIR-compatible formats for interoperability
  • Template IRB applications and data use agreements included with enterprise plans
  • Tiered API pricing starting at $199/month for country-level aggregated data
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Data Points Available

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Facilities Contributing

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API Requests Served

Ready to Transform Your SCD Program?

Join hundreds of organizations already using Tracka to improve patient outcomes across Africa.