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NCT04920890
Radiofrequency Intervention in Neurological Pathologies Post COVID-19
NA trial testing Radiofrequency therapy with manual therapy in Covid19 in 10 participants. Completed in 20 July 2022.
21 June 2022
Quick facts
| Lead sponsor | Clinica Gema Leon |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 10 |
| Start date | 16 June 2021 |
| Primary completion | 21 June 2022 |
| Estimated completion | 20 July 2022 |
| Sites | 1 location across Spain |
Drugs / interventions tested
- Radiofrequency therapy with manual therapy
Conditions studied
- Covid19 — all drugs for Covid19 →
- Neurological Injury — all drugs for Neurological Injury →
- Olfactory Disorder — all drugs for Olfactory Disorder →
- Gustatory Agnosia — all drugs for Gustatory Agnosia →
Sponsor
Clinica Gema Leon
Who can join
Eligibility, any sex, with Covid19 or Neurological Injury. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The sequelae that occur in post-COVID-19 patients are multiple and, at a therapeutic level, these represent a new challenge within the general context of the pandemic that the world is suffering. The virus has managed to end thousands of lives today and many other cases are being charged as directly responsible for a multiplicity of multi-system damages that need to be diagnosed and treated. Among the most relevant, are those that can affect to neurological levels in patients without previous pahologies, and in patients at risk who already had a pathology prior to infection. On the other hand, signs and symptoms have been observed characteristic in the organ systems described above in post-contagion patients, directly associated with sequelae SARV-CoV2. The radio frequency (RF) of electromagnetic waves represents a technology of proven efficacy and safety in multiple fields of both human and veterinary medicine. These include neurological pathologies, and very especially those that affect the locomotor system. In therapeutics there are different RF modalities depending on the modality, polarity, type of signal and frequency, which in turn translate into different therapeutic profiles, clinical indications, efficacy and safety. Among the RF technologies most used today and that have a greater scientific background, is the one known as Resistive Capacitive Monopolar Radio Frequency at 448 kHz (INDIBA®) (RFMCR). This study aims to assess the efficacy and safety of RFMCR in the treatment of neurological sequelae in patients presenting this type of pathologies that appear after contagion by COVID-19. Through this non-invasive technique, the investigators want to show that RF can help the physical rehabilitation of these patients through metabolic stimulation, increased vascularization and oxygenation of directly affected tissues, effects of deep hyperthermia generated by the interaction of the current with the treated biological substrate, as well as the activation of tissue regeneration, the result of subthermal action. It is thus intended to improve signs such as lung capacity, dyspnea, neuropathies and global muscle capacity, which are essential for the recovery of the post-COVID-19 patients. The hypothesis of this study is that current post-COVID-19 treatments can be significantly improved in order to prevent complications and ensure the patients' well-being.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04920890
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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- NCT05013632 — COVID-19 International Drug Pregnancy Registry · recruiting
- NCT04806061 — Urine Alkalinisation in COVID-19 · NA · active not recruiting
Other Clinica Gema Leon trials
Trials by the same sponsor.
- NCT06544395 — Efficacy of Non-invasive Neuromodulation Treatments for COVID-19 Sequelae · NA · not yet recruiting
- NCT05340049 — Craniosacral Therapy Improves Infant Neurodevelopment · NA · completed
- NCT05190029 — Craniosacral Test and Primitive Reflexes in Infant Neurodevelopment · NA · completed
- NCT05167162 — Efficacy of the Most Commonly Used Physiotherapeutic Treatments for Acute Lower Limb Fatigue in Athletes · NA · completed
- NCT05002504 — Craniosacral Therapy Children's, Balance-Coordination · NA · completed
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 NCT04920890 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Clinica Gema Leon
- Last refreshed: 15 June 2025
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/NCT04920890.
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