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Reversal of Neuromuscular Blockade and Perioperative Arrhythmias - Trial NCT04720573

Access comprehensive clinical trial information for NCT04720573 through Pure Global AI's free database. This phase not specified trial is sponsored by Basaksehir Cam & Sakura ลžehir Hospital and is currently Completed. The study focuses on Neuromuscular Blockade. Target enrollment is 80 participants.

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NCT04720573
Completed
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Trial Details
ClinicalTrials.gov โ€ข NCT04720573
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Reversal of Neuromuscular Blockade and Perioperative Arrhythmias
Influence of the Neuromuscular Blockade and Its Reversal on Perioperative Arrhythmias

Study Focus

Neuromuscular Blockade

Neostigmine

Interventional

drug

Sponsor & Location

Basaksehir Cam & Sakura ลžehir Hospital

Istanbul, Turkey

Timeline & Enrollment

N/A

Jun 01, 2019

Nov 01, 2019

80 participants

Primary Outcome

Significant arrhythmic event

Summary

Patients scheduled for elective abdominopelvic laparoscopic surgery under general anesthesia
 were included. Rocuronium was used for the neuromuscular blockade (NMB) and the level of NMB
 was monitored with train-of-four (TOF) measurements. The participants from whom informed
 consent had been received were allocated to two groups according to the agent used for
 reversal of NMB, sugammadex, or neostigmine. The ECG recordings of the subjects were followed
 with a rhythm Holter device throughout the procedure until the postoperative 12th hour.
 Additionally, preoperative and immediate postoperative 12-lead ECGs were evaluated for
 corrected QT calculations and QT dispersion. Proarrhythmogenicity was assessed with QT
 related measurements. The documented arrhythmic events on the Holter monitoring were
 designated as clinical end-points.

ICD-10 Classifications

Skeletal muscle relaxants [neuromuscular blocking agents]
Poisoning: Skeletal muscle relaxants [neuromuscular blocking agents]
Other neuromuscular dysfunction of bladder
Neuromuscular dysfunction of bladder, unspecified
Neuromuscular scoliosis

Data Source

ClinicalTrials.gov

NCT04720573

Non-Device Trial