Post-viral / Immune

Long COVID: cell-therapy evidence and registered trials

A source-first research page for the exact condition. It does not recommend a cell product, clinic or private treatment.

Registry snapshot

ClinicalTrials.gov returned 11 registered studies for the stored condition/intervention query, including 2 recruiting records, retrieved 2026-08-05T06:02:03+00:00. A registry count does not establish efficacy, approval, relevance or eligibility; inspect each study's design, product, status and inclusion criteria.

Research activity over time

10 studies were newly registered in 2021–2025. The first study in this registry query was posted in 2021; the registry now holds 11 in total, of which 2 are recruiting. Counting is by first-posted date, so the series reflects when research was registered — not enrolment, completion or results.

Newly registered Long COVID studies by year
20214
20221
20233
20242
20261

Source: ClinicalTrials.gov API v2, retrieved 2026-08-05. A registration count is not evidence of efficacy, approval or eligibility. Open the exact query ↗

What to verify before interpreting a study or offer

  1. The exact product, cell source, processing, dose and delivery route.
  2. The indication, study phase, comparator, endpoints, status and eligibility criteria.
  3. Whether the proposed use is authorised, part of a registered trial or otherwise investigational.
  4. Provider and manufacturing authorisations, release testing, traceability and adverse-event reporting.
  5. How the proposal compares with current standard care, reviewed by an independent physician.

Sources & further reading

Registry data is a discovery aid, not evidence that a treatment works or is suitable for an individual patient.

Compare cell-therapy evidence, registered studies and published price observations.

StemCellAtlas is a source-first research and cost-planning guide. It separates registry and regulator evidence from heterogeneous commercial observations.

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