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NCT04941664

Minimum Effective Local Anesthetic Volume for Ultrasound Guided Superior Trunk Block

Recruiting now NA Last updated 13 April 2025
What this trial tests

NA trial testing 0.5% levobupivacaine in Musculoskeletal Diseases or Conditions in 25 participants. Currently enrolling.

Timeline
19 January 2023
Primary endpoint
31 July 2026
31 August 2026

Quick facts

Lead sponsorChinese University of Hong Kong
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment25
Start date19 January 2023
Primary completion31 July 2026
Estimated completion31 August 2026
Sites1 location across Hong Kong

Drugs / interventions tested

Conditions studied

Sponsor

Chinese University of Hong Kong

Who can join

Adults 18 to 75, any sex, with Musculoskeletal Diseases or Conditions. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to identify the minimum effective dosage of a commonly used local anaesthetic drug "levobupivacaine" required to produce an effective ultrasound guided (USG) superior trunk block (STB) in at least 90% of patients for shoulder arthroscopic surgeries.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of 0.5% levobupivacaine

Trials testing the same drug.

Other recruiting trials for Musculoskeletal Diseases or Conditions

Currently open trials in the same condition.

Other Chinese University of Hong Kong trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT04941664.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing