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NCT06118138
Hyperbaric High Pressure Oxygen Therapy in Post-COVID Syndrome and ME/CFS
trial testing Hyperbaric oxygen therapy (HBOT) in Post-COVID ME/CFS in 60 participants. Completed in 31 December 2025.
31 December 2025
Quick facts
| Lead sponsor | Charite University, Berlin, Germany |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 60 |
| Start date | 15 July 2023 |
| Primary completion | 31 December 2025 |
| Estimated completion | 31 December 2025 |
| Sites | 1 location across Germany |
Drugs / interventions tested
- Hyperbaric oxygen therapy (HBOT)
Conditions studied
- Post-COVID ME/CFS — all drugs for Post-COVID ME/CFS →
Sponsor
Charite University, Berlin, Germany
Who can join
Adults 18 to 65, any sex, with Post-COVID ME/CFS. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The objective of this observational study is to document symptom progression in 60 patients with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) who undergo Hyperbaric Oxygen Therapy (HBOT) following COVID or other infections. Participants will receive HBOT treatment as an additional option after completing the Chronic Fatigue Syndrome CARE (CFS\_CARE) study and will be invited to take part in this observational study. Patients will complete health evaluations in the form of questionnaires, including the 36-Item Short Form Health Survey (SF-36), to assess changes in ME/CFS-related symptoms after HBOT. Rather than evaluating the efficacy of HBOT itself, the study will focus on observing and documenting these changes. Its goal is to offer valuable insights into symptom progression in ME/CFS patients receiving HBOT, which can serve as a foundation for future interventional randomized controlled trials.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Hyperbaric oxygen therapy improves clinical symptoms and functional capacity and modulates thalamic connectivity in ME/CFS: a prospective cohort study.
Kim L, Cammà G, Peters CK, Mantwill M, et al · · 2026 · PMID 42249466 · DOI 10.1186/s12967-026-08324-6
Verify or expand the search:
- PubMed search for NCT06118138
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
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Related trials
Other recruiting trials for Post-COVID ME/CFS
Currently open trials in the same condition.
- NCT05697640 — Study to Investigate Improvement in Physical Function in SF-36 With Vericiguat Compared With Placebo in Participants Wit · Phase 2 · active not recruiting
Other Charite University, Berlin, Germany trials
Trials by the same sponsor.
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- NCT07476729 — International Study for Treatment of Childhood Relapsed Precursor B-Cell ALL 2020 (IntReALL BCP 2020) · Phase 3 · not yet recruiting
- NCT07503054 — Ovarian Cancer Screening and AI · NA · not yet recruiting
- NCT07529197 — Observational Study on Immunoadsorption (IA) in Patients With Autoantibody-Positive Post-Infectious ME/CFS · recruiting
- NCT07388693 — Feasibility of Integrating Olfactory Stimuli Into Virtual Reality Cue Exposure for Patients With Alcohol Dependence · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06118138 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Charite University, Berlin, Germany
- Last refreshed: 15 April 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06118138.
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