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NCT04457557
Local Anesthetic Concentration and Rebound Pain
NA trial testing Reduced concentration of local anesthetic (ropivacaine) in Rebound Pain in 60 participants. Status unknown.
30 June 2023
Quick facts
| Lead sponsor | Ajou University School of Medicine |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 10 July 2020 |
| Primary completion | 30 June 2023 |
| Estimated completion | 31 July 2023 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Reduced concentration of local anesthetic (ropivacaine)
- Usual concentration of local anesthetic (ropivacaine)
Conditions studied
- Rebound Pain — all drugs for Rebound Pain →
Sponsor
Ajou University School of Medicine
Who can join
Adults 19 to 70, any sex, with Rebound Pain. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The rebound pain after nerve block could interfere with patient's recovery and rehabilitation. It is not known how local anesthetic concentrations affect rebound pain. The aim of this study is evaluation of the effect of local anesthetic concentration on rebound pain after interscalene block for shoulder surgery.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04457557
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Rebound Pain
Currently open trials in the same condition.
- NCT07196631 — Comparison of Liposomal Bupivacaine Versus Ropivacaine in Alleviating Rebound Pain · Phase 4 · active not recruiting
- NCT06382896 — Effect of Oliceridine on Rebound Pain · recruiting
Other Ajou University School of Medicine trials
Trials by the same sponsor.
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- NCT06964217 — Immediate Fracture Risk After Antihypertensive Drug Initiation · not yet recruiting
- NCT05751603 — Effectiveness on Smooth Extubation According to the Administration Time of Sugammadex · NA · not yet recruiting
- NCT07479160 — Heart to Heart Web-based Communication Program for Heart Failure · 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 NCT04457557 (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 Ajou University School of Medicine
- Last refreshed: 30 September 2022
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/NCT04457557.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing