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NCT03476694
Ultrasound Guided Supraclavicular Brachial Plexus Block, Volume Comparison of Local Anaesthetics and Diaphragmatic Motility.
Phase 4 trial testing ultra sound guided supraclavicular brachial plexus block in Sucessful Block With Less Hemidiaphragmatic Paresis in Distal Upper Arm Fracture in 60 participants. Status unknown.
1 February 2019
Quick facts
| Lead sponsor | B.P. Koirala Institute of Health Sciences |
|---|---|
| Phase | Phase 4 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 1 July 2018 |
| Primary completion | 1 February 2019 |
| Estimated completion | 1 February 2019 |
| Sites | 1 location across Nepal |
Drugs / interventions tested
- ultra sound guided supraclavicular brachial plexus block
Conditions studied
- Sucessful Block With Less Hemidiaphragmatic Paresis in Distal Upper Arm Fracture — all drugs for Sucessful Block With Less Hemidiaphragmatic Paresis in Distal Upper Arm Fracture →
Sponsor
B.P. Koirala Institute of Health Sciences
Who can join
Adults 18 to 60, any sex, with Sucessful Block With Less Hemidiaphragmatic Paresis in Distal Upper Arm Fracture. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Brachial plexus block as done by landmark technique use large volume of local anaesthetics (at least 30-40 ml), leading to higher incidence of phrenic nerve involvement and diaphragmatic dysfunction. With use of ultrasound dose of local anaesthetic can be reduced. Volume as low as 20 ml when use by ultrasound guidance has shown to provide successful block with no hemidiaphragmatic palsy when compared with nerve stimulation technique. But no study has compared the different volumes of drug on success rate and diaphragmatic motility.So in this study , the investigators want to compare the incidence of hemidiaphragm paralysis and success of block with different volumes of local anaesthetic , so that the lowest effective dose with higher safety profile can be determined.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT03476694
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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 NCT03476694 (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 B.P. Koirala Institute of Health Sciences
- Last refreshed: 29 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/NCT03476694.
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