Sugammadex Efficacy and Safety for Reversal of Pipecuronium-induced Neuromuscular Blockade

Adult Subjects Undergoing Abdominal Surgery Under General Anesthesia Clinical Trial

Official title:

Randomized, Parallel-group, Placebo-controlled, Safety-assessor Blinded Trial in Adult Subjects Evaluating the Efficacy and Safety of Sugammadex for Reversal of Pipecuronium-induced Neuromuscular Blockade in Subjects Undergoing Abdominal Surgery Under General Anesthesia

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT01424488
• Other study ID #: CCHRussianRailways
• Status: Not yet recruiting
• Phase: Phase 4
• First received: August 22, 2011
• Last updated: August 26, 2011
• Start date: September 2011
• Est. completion date: February 2012

Study information

• Verified date: August 2011
• Source: Central Clinical Hospital #1 of LLC Russian Railways
• Contact: Eduard Nikolaenko, MD PhD
• Phone: +7 495 490 1216
• Email: ednicolayenko[@]yahoo.com, Evgenia.Bukharova[@]merck.com
• Is FDA regulated: No
• Health authority: Russia: Independent Ethic Committee of CCHRussianRailways
• Study type: Interventional

Clinical Trial Summary

Primary objectives:

1. to investigate the efficacy of sugammadex in dose of 4 mg/kg administered at reappearance of T2 for reversal of pipecuronium-induced neuromuscular blockade in subjects undergoing abdominal surgery under general anesthesia

2. to evaluate the safety and tolerability of a single dose of 4 mg/kg sugammadex administered at reappearance of T2 for reversal of pipecuronium-induced neuromuscular blockade

Secondary objectives:

1. to evaluate the time from the start of sugammadex or placebo administration to the time of extubation and to the time of recovery of TOF ratio to ≥ 0.9

Exploratory objectives:

1. to evaluate the Operating Room (OR) and Post Anesthetic Care Unit (PACU) length of stay after the end of surgery in subjects with pipecuronium induced neuromuscular blockade reversed by 4.0 mg.kg-1 sugammadex compared to placebo (saline)

2. compare the number of patients extubated in the OR after the reversal by sugammadex or placebo, evaluate the TOF ratio at the time of extubation

Clinical hypothesis:

1. Sugammadex has to be effective and well tolerated for reversal of pipecuronium-induced blockade

Description:

Sugammadex is the first selective relaxant binding agent indicated for reversal of rocuronium and vecuronium-induced blockade.

At the same time sugammadex is able to form the complexes with other aminosteroid-based muscle relaxants including long acting NMBAs* such as pancuronium 1,2.

Still there are only limited data on the efficacy of sugammadex with pancuronium and no data on the efficacy of sugammadex with other aminosteroid-based long acting NMBA - pipecuronium which is still widely used in Russia (as well as in the other former Soviet Union Countries and Eastern Europe countries). In the only study evaluating efficacy of sugammadex with pancuronium has been shown that moderate pancuronium-induced blockade is effectively reversed in less than 3 minutes with a sugammadex dose of 4.0 mg/kg 3. In this respect it would be interesting in this study to evaluate the efficacy of sugammadex with pipecuronium.

It is also very well known that the incidence of postoperative residual blockade (and its complications) is higher when the long acting NMBAs such as pancuronium and pipecuronium are used 4,5,6,7. So the possibility to use sugammadex for reversal of pipecuronium-induced blockade could help to reduce the incidence of residual blockade and related complications.

The effectiveness of sugammadex for the reversal of long acting NMBAs such as pipecuronium at the same time would be significant in light of the limitations of cholinesterase inhibitors. These drugs are more often administered after the long acting NMBAs taking into account their prolonged clinical duration of action.

It is expected that the dose of sugammadex 4 mg/kg will allow to recover the TOF ratio to 0.9 in less than 4 min and in this case this time will be similar to the recovery time after moderate pancuronium-induced blockade.

*NMBAs-neuromuscular blocking agents

2.3 Study Design

1. A single center, randomized, parallel-group, placebo-controlled, safety-assessor (single) blinded trial

2. Adult patients undergoing abdominal surgery under general anesthesia who receive succinylcholine for tracheal intubation and pipecuronium for maintenance of neuromuscular blockade. Planned number of subjects - 42

3. Patients will be randomised into 2 groups to receive at the end of surgery 4 mg/kg of sugammadex or 3 ml of saline (placebo) for reversal of pipecuronium-induced neuromuscular blockade. According to the sample size justification randomization will be done with the ratio of 1:2 - 14 patients will be enrolled in the placebo group and 28 patients - in sugammadex group

4. Neuromuscular function will be monitored using the objective neuromuscular monitoring with the TOF-Watch® SX acceleromyograph at the adductor pollicis muscle, starting after induction of anesthesia (before succinylcholine and pipecuronium administration) and continuing at least until recovery of the TOF ratio to 0.9

5. The primary efficacy variable is the time from the start of sugammadex or placebo administration (reappearance of T2) to recovery of the TOF ratio to 0.9

6. The secondary efficacy variable is the time from the start of sugammadex or placebo administration to the time of extubation

7. Safety assessment is going to be done in order to evaluate the safety and tolerability of sugammadex for reversal of pipecuronium-induced neuromuscular blockade (analysis of AEs and vital signs)

Safety variables:

• Vital signs, i.e. heart rate and blood pressure (at screening, pre-pipecuronium, pre-sugammadex or pre-placebo, at 2, 5, 10, and 30 minutes post-sugammadex or post-placebo, and at the post-anesthetic visit)

• Physical examination (at screening, at the post-anesthetic visit)

• Pre-treatment (serious) events (from signing informed consent until administration of sugammadex or placebo) and (serious) adverse events ((S)AEs, from administration of sugammadex or placebo up to the end of trial)

8. Descriptive Variables:

• Time from OR admission (physical placement of subject into the OR) to actual OR discharge

• Time from start of sugammadex or placebo administration to actual OR discharge

• Time from tracheal extubation to actual OR or PACU discharge

• Time from PACU admission to actual PACU discharge

• Number of patients extubated in the OR in both groups

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 42
• Est. completion date: February 2012
• Est. primary completion date: February 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subjects of ASA class 1-3

• Subjects of age = 18 years

• Subjects undergoing abdominal surgery under general anesthesia who receives succinylcholine for tracheal intubation and pipecuronium for maintenance of neuromuscular blockade

• Subjects who have given written informed consent

Exclusion Criteria:

• Subjects in whom a difficult intubation is expected

• Subjects known or suspected to have neuromuscular disorders affecting NMB

• Subjects known or suspected to have a significant renal dysfunction or a severe hepatic dysfunction

• Subjects known or suspected to have (family) history of malignant hyperthermia

• Subjects known or suspected to have an allergy to opioids, muscle relaxants or other medication used during general anesthesia

• Female subjects who are pregnant

• Female subjects who are breast-feeding

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Adult Subjects Undergoing Abdominal Surgery Under General Anesthesia

Intervention

Drug:
• sugammadex
Anesthetised patients will receive a single intubation dose of succinylcholine (1.0 mg/kg) and maintenance bolus dose of pipecuronium (0.08 mg/kg) to maintain the level of neuromuscular blockade at reappearance of T2 Sugammadex in the dose of 4 mg/kg is to be administered as an intravenous bolus dose at the level of neuromuscular blockade of reappearance of T2 (moderate blockade) by means of TOF-Watch SX after the last dose of pipecuronium according to randomization
• placebo
Anesthetised patients will receive a single intubation dose of succinylcholine (1.0 mg/kg) and maintenance bolus dose of pipecuronium (0.08 mg/kg) to maintain the level of neuromuscular blockade at reappearance of T2. 3,0 ml of saline (placebo) is to be administered as an intravenous bolus dose at the level of neuromuscular blockade of reappearance of T2 (moderate blockade) by means of TOF-Watch SX after the last dose of pipecuronium according to randomization

Locations

Country	Name	City	State
Russian Federation	Central Clinical Hospital #1 of LLC "Russian Railroad"	Moscow

Sponsors (1)

Lead Sponsor	Collaborator
Central Clinical Hospital #1 of LLC Russian Railways

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	time from the start of sugammadex or placebo administration (reappearance of T2) to recovery of the TOF ratio to 0.9	measurement of time from the start of sugammadex or placebo administration (reappearance of T2) to recovery of the TOF ratio to 0.9	during peri-anesthetic period (after the surgery and until 10 hours after the surgery)	Yes
Secondary	time from the start of sugammadex or placebo administration to the time of extubation	measurement of time from the start of sugammadex or placebo administration to the time of extubation	during peri-anesthetic period (after the surgery and until 10 hours after the surgery	Yes