Overview
Rocuronium (rapid onset-curonium) is a desacetoxy analogue of vecuronium with a more rapid onset of action. It is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia, to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. Introduced in 1994, rocuronium has rapid onset, and intermediate duration of action. It is commonly marketed under the trade names Zemuron and Esmeron. The drug is associated with the risk of developing allergic reactions in some high-risk patients, such as those with asthma. However, there was a similar incidence of allergic reactions associated with other non-depolarizing neuromuscular blocking agents. Sugammadex is a γ-cyclodextrin derivative that has been introduced as a novel agent to reverse the action of rocuronium.
Indication
For inpatients and outpatients as an adjunct to general anesthesia to facilitate both rapid sequence and routine tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.
Associated Conditions
- Muscle fasciculation caused by succinylcholine
Research Report
Rocuronium Bromide: A Comprehensive Pharmacological and Clinical Monograph
1.0 Executive Summary
Rocuronium is an aminosteroid, nondepolarizing neuromuscular blocking agent (NMBA) distinguished in modern anesthetic practice by its characteristically rapid onset of action and intermediate duration.[1] As a cornerstone of anesthesia, it is employed as an adjunct to general anesthesia to facilitate both routine and rapid sequence tracheal intubation (RSI), as well as to provide profound skeletal muscle relaxation during surgical procedures and for patients requiring mechanical ventilation.[3] Its primary clinical advantage lies in its ability to achieve intubating conditions at a speed comparable to the depolarizing agent succinylcholine, particularly when administered at higher doses, but with a more favorable and safer side-effect profile, establishing it as a critical alternative for RSI.[5]
A transformative development in the clinical use of rocuronium has been the introduction of sugammadex, a selective relaxant binding agent (SRBA). While the neuromuscular blockade induced by rocuronium can be partially reversed by traditional acetylcholinesterase inhibitors like neostigmine, sugammadex offers a unique mechanism that allows for rapid, complete, and reliable reversal of even deep levels of blockade.[1] This innovation has profoundly enhanced the safety profile and clinical utility of rocuronium, allowing for more aggressive dosing with a reliable safety net.[7]
Clinical Trials
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Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2015/09/11 | Not Applicable | Completed | Brno University Hospital | ||
2015/09/03 | Not Applicable | Completed | Aydin Adnan Menderes University | ||
2015/07/01 | Not Applicable | Completed | |||
2015/06/29 | Phase 4 | Completed | Centro Hospitalar do Porto | ||
2015/06/15 | Not Applicable | Completed | |||
2015/06/12 | Phase 2 | Completed | |||
2015/06/10 | Phase 4 | UNKNOWN | |||
2015/06/08 | Phase 4 | UNKNOWN | |||
2015/05/21 | Phase 4 | Completed | |||
2015/04/13 | Phase 4 | Completed |
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