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NCT03572686
Dexamethasone at Lower Concentration Ropivacaine in the Supraclavicular Nerve Block
NA trial testing Ropivacaine 0.5% 20mL in Analgesia in 90 participants. Status unknown.
31 December 2020
Quick facts
| Lead sponsor | Kaohsiung Medical University Chung-Ho Memorial Hospital |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | other |
| Enrollment | 90 |
| Start date | 13 April 2018 |
| Primary completion | 31 December 2020 |
| Estimated completion | 31 December 2020 |
| Sites | 2 locations across Taiwan |
Drugs / interventions tested
- Ropivacaine 0.5% 20mL — full drug profile →
- Ropivacaine 0.25% 20ml — full drug profile →
- Ropivacaine 0.25% 20ml + dexamethasone 8mg — full drug profile →
Conditions studied
- Analgesia — all drugs for Analgesia →
- Motor Activity — all drugs for Motor Activity →
- Brachial Plexus Block — all drugs for Brachial Plexus Block →
Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
Who can join
Adults 20 to 75, any sex, with Analgesia or Motor Activity. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The supraclavicular brachial plexus block is widely used in upper limb surgery below the shoulder. However, this can easily lead to long-term motor nerve blockage, Horner's syndrome, phrenic nerve paralysis or systemic poisoning, and even serious side effects such as cardiac arrest. Dexamethasone is a synthetic corticosteroid and becoming more common to use steroids as an adjunct to local anesthetics in brachial plexus block. In order to reduce the incidence of long-acting topical anesthetics from the nerve block in the supraclavicular arm, reducing the local anesthetic concentration is a feasible method, but this will also result in a shorter time to neurological block. The investigators hypothesized that the addition of Dexamethasone 5 mg to low concentrations (0.25%) of Ropivacaine would prolong postoperative analgesia.Therefore, the purpose of this study was to compare the postoperative analgesia and the side effects of postoperative supraclavicular brachial plexus blockade with the addition of Dexamethasone 5mg to Ropivacaine (0.5%) alone and Ropivacaine (0.25%) in low concentrations.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT03572686
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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 NCT03572686 (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 Kaohsiung Medical University Chung-Ho Memorial Hospital
- Last refreshed: 28 June 2018
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/NCT03572686.
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