CompletedPhase 4

The Prevention of Pain Associated With Rocuronium Injection

150 participantsStarted 2014-05

Plain-language summary

The purpose of this study is to determine whether efficacy of different doses of lidocain and acetaminophen for the prevention of rocuronium injection pain and frequency of withdrawal movements during the general anesthesia induction period.

Who can participate

Age range18 Years – 70 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18- 70 years of ASA physical status I- II who were to undergo various elective operations. Exclusion Criteria: * Patients with chronic pain syndrome, * Patients with neurologic deficits, * Patients with thrombophlebitis, * Patients with difficult venous access, * Patients with allergy

What they're measuring

Change in intraoperative pain

Timeframe: 10 seconds

Trial details

NCT IDNCT02524743

SponsorSuleyman Demirel University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2014-09

View on ClinicalTrials.gov More Injection Site Irritation trials