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NCT07285980: BBLP

Comparison of Bier Block and Lidocaine-Propofol Mixture for Prevention of Propofol Injection Pain

Completed NA Last updated 26 December 2025
What this trial tests

NA trial testing propofol in Propofol Injection Pain in 180 participants. Completed in 31 July 2025.

Timeline
1 March 2025
Primary endpoint
31 July 2025
31 July 2025

Quick facts

Lead sponsorAsma Ladib
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment180
Start date1 March 2025
Primary completion31 July 2025
Estimated completion31 July 2025
Sites1 location across Tunisia

Drugs / interventions tested

Conditions studied

Sponsor

Asma Ladib — full company profile →

Who can join

18 and older, any sex, with Propofol Injection Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial was to evaluate methods to prevent pain on intravenous administration of propofol during induction of anesthesia. Propofol frequently causes a burning or painful sensation when injected into a peripheral vein. This randomized study compared three approaches in adult patients scheduled for elective surgery: propofol alone (control), propofol with 40 mg lidocaine mixed directly, and a brief intravenous lidocaine under venous occlusion (Bier block) using 40 mg for 2 minutes before propofol. The primary outcome was the incidence of pain on propofol injection measured with a 4-point verbal rating scale (0 = no pain to 3 = severe pain). Secondary outcomes included pain intensity, peri-induction hemodynamic parameters, and local injection-site adverse effects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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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/NCT07285980.

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