Summary
Device is tracked by OSMF as an investigational option for Long COVID; no regulator has approved it for this indication, and most post-viral conditions have no approved disease-modifying therapy at all. ClinicalTrials.gov lists 1 registered trial linking Device to Long COVID: 1 has completed. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 88 participants. Registered activity dates to 2023. The literature layer holds 18 publications for this pair: 8 clinical trial publications and 10 other publications. These are primary trial reports rather than syntheses, so results have not yet been pooled or graded independently.
Long COVID / PASC is tracked on the OSMF post-viral programme alongside ME/CFS, Long COVID, POTS and MCAS. Across the programme, 423 candidate agents are logged for Long COVID, most of them preliminary; this page isolates the record for one of them.
Evidence table
| Evidence tier | C · Preliminary |
|---|---|
| Evidence score | 33.5 (trials 2.5, literature 26.0, tier 5, approved bonus 0.0) |
| Registered trials | 1 total: 0 recruiting, 0 active / not yet recruiting, 1 completed, 0 other |
| Linked publications | 18 (10 other publications, 8 clinical trial publications) |
| Agent type | Device (Medical Device) |
| Development stage (any indication) | Investigational |
| Mechanism / class | Not recorded |
| Data sources | OSMF therapeutic agent database, ClinicalTrials.gov, PubMed |
How the evidence score is calculated
- Each registered trial scores by status (recruiting / active / enrolling 3, completed 2.5, not yet recruiting 2, unknown 1, terminated / withdrawn / suspended 0.5) plus a phase bonus (phase 3-4 +2, phase 2 +1, phase 1 +0.5). The trial component is capped at 30.
- Each literature item scores by design (Cochrane review 5, meta-analysis 4, systematic review 3, RCT 3, clinical trial publication 2, curated reference 1.5, other PubMed record 1). The literature component is capped at 30.
- The existing evidence tier adds 15 (A / Strong), 10 (B / Moderate), 5 (C / Preliminary) or 0 (D / Anecdotal).
- Agents approved for any indication (max clinical phase 4) add 5, because an approved agent has an established safety profile that lowers the barrier to repurposing trials.
- The score ranks what has been studied, not what works. It does not read effect sizes or directions of effect.
Registered clinical trials
| NCT ID | Title | Status | Phase | Enrolment |
|---|---|---|---|---|
| NCT05817006 | Research of the Long-COVID-19 Syndrome in the Children Samara State Medical University · 2023 | completed | Not applicable | 88 |
Published literature
- Clinical trial publication (PubMed validation search) PubMed record PMID 41906071
- Clinical trial publication (PubMed validation search) PubMed record PMID 40810942
- Clinical trial publication (PubMed validation search) PubMed record PMID 40696212
- Clinical trial publication (PubMed validation search) PubMed record PMID 40097846
- Clinical trial publication (PubMed validation search) PubMed record PMID 39969545
- Clinical trial publication (PubMed validation search) PubMed record PMID 39516528
- Clinical trial publication (PubMed validation search) PubMed record PMID 39095520
- Clinical trial publication (PubMed validation search) PubMed record PMID 38752418
- Review (PubMed validation search) PubMed record PMID 38775379
- Review (PubMed validation search) PubMed record PMID 36671900
- Review (PubMed validation search) PubMed record PMID 23109544
- Case series (PubMed validation search) PubMed record PMID 40190996
- Case series (PubMed validation search) PubMed record PMID 36714125
- Case report (PubMed validation search) PubMed record PMID 39257640
- Case report (PubMed validation search) PubMed record PMID 37767178
- Case report (PubMed validation search) PubMed record PMID 35310731
- Case report (PubMed validation search) PubMed record PMID 35006516
- Case report (PubMed validation search) PubMed record PMID 34692373
Mechanism and notes
This is a device or procedure-based intervention; no pharmacological mechanism is recorded.
Clinical notes: Investigational for listed conditions. 1 associated trial(s) and 0 study reference(s) in current data. Review primary sources and consult specialists before use.
Safety: Limited specific safety data in these populations. Review full prescribing information and consult specialist. Many agents used off-label or investigational.
Dosing in studies: See linked studies/trials for reported doses and durations; typical protocols vary widely.
Frequently asked questions
Is Device approved for Long COVID?
Device is tracked by OSMF as an investigational option for Long COVID; no regulator has approved it for this indication, and most post-viral conditions have no approved disease-modifying therapy at all. Approval status for the specific indication should always be confirmed with the relevant regulator and prescribing information.
Is Device in clinical trials for Long COVID?
ClinicalTrials.gov lists 1 registered trial linking Device to Long COVID: 1 has completed. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 88 participants. Registered activity dates to 2023.
What does the evidence show for Device in Long COVID?
Device has 1 completed trial and 18 linked publications for Long COVID. Completed trials may or may not have posted results; follow the NCT links to check. OSMF's existing evidence tier for this pair is C (Preliminary), taken from the OSMF therapeutic agent database, which grades agents by the volume and design of condition-specific evidence rather than by effect size.
Cite this page
Data: ClinicalTrials.gov, PubMed, Open Targets, ChEMBL, DGIdb and the OSMF therapeutic agent database. Last updated 2026-10-07. Page built 2026-10-07.