WHO ICTRP trial

To evaluate the efficacy of pretreatment of vein with plain intravenous…

CTRI/2024/04/065103 · Clinical Trials Registry India (CTRI) · Not Recruiting

Key facts

Trial ID CTRI/2024/04/065103
Public title To evaluate the efficacy of pretreatment of vein with plain intravenous lignocaine before propofol with that of premixed solution of lignocaine and propofol to decrease pain on injection during propofol induction of anaesthesia:
Scientific title Comparison of the efficacy of pretreatment of vein with plain intravenous lignocaine before propofol with that of premixed solution of lignocaine and propofol to decrease pain on injection during propofol induction of anaesthesia: a prospective, randomized double blind study. - NA
Primary sponsor NIL
Registry Clinical Trials Registry India (CTRI)
Recruitment status Not Recruiting
Study type Interventional
Countries India
Conditions Health Condition 1: I999- Unspecified disorder of circulatory system
Interventions Intervention1: Group A will receive study drug 1 with 10 ml of NS before tourniquet application and then study drug 2 with 10 ml of Propofol mixed with 1ml of intravenous Lignocaine will be administered. Total volume of study drug 1 is 10…
Registration date Feb 4, 2024
Target size 120
Secondary IDs NIL
Registry page ctri.nic.in

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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