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NCT03773198: ERESCAO
Effectiveness of Energy Resonance by Skin Stimulation in the Management of Anxious Patients Who Require Scheduled Orthopaedic Surgery
Phase 3 trial testing Energy Resonance through Cutaneous Stimulation in Patient Requiring Scheduled Conventional Orthopedic Surgical Intervention of the Upper or Lower Limb in 86 participants. Completed in 12 May 2023.
12 May 2023
Quick facts
| Lead sponsor | Centre Hospitalier Universitaire Dijon |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | other |
| Enrollment | 86 |
| Start date | 5 April 2019 |
| Primary completion | 12 May 2023 |
| Estimated completion | 12 May 2023 |
| Sites | 1 location across France |
Drugs / interventions tested
- Energy Resonance through Cutaneous Stimulation
- questionnaires
Conditions studied
- Patient Requiring Scheduled Conventional Orthopedic Surgical Intervention of the Upper or Lower Limb — all drugs for Patient Requiring Scheduled Conventional Orthopedic Surgical Intervention of the Upper or Lower Limb →
Sponsor
Centre Hospitalier Universitaire Dijon
Who can join
18 and older, any sex, with Patient Requiring Scheduled Conventional Orthopedic Surgical Intervention of the Upper or Lower Limb. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The need for a surgical procedure may cause a patient to experience reactive anxiety. This reaction is appropriate if it is of low to moderate intensity. On the other hand, various studies have shown that postoperative awakening is more complicated if the patient experiences major preoperative anxiety. Thus, reducing anxiety could be a tool for preventing chronic pain. For several years now, the investigator's facility has been implementing Energy Resonance through Cutaneous Stimulation (ERCS), a method based on "listening" to the body's vibrations through the fingers on points based on the mapping of meridians in Chinese medicine. ERCS practitioners have noted the benefits of this method, particularly in soothing patients. It therefore seems necessary to detect and manage this anxiety beforehand and ERCS seems appropriate in this situation.
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 NCT03773198
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT03773198 (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 Centre Hospitalier Universitaire Dijon
- Last refreshed: 7 December 2023
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/NCT03773198.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing