Last Updated: July 26, 2026

CLINICAL TRIALS PROFILE FOR PIPECURONIUM BROMIDE


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All Clinical Trials for pipecuronium bromide

Trial ID Title Status Sponsor Phase Start Date Summary
NCT05693428 ↗ Influence of Anesthetics on Clinical Outcome During Cardiac Surgery in Adults Completed Astana Medical University N/A 2022-01-22 Abstract Cardiac surgery in adults is associated with the occurrence of post-operative complications. Even minor complications can increase the cost of their treatment. Given the potentially preventable nature of a number of these postoperative complications, preventive methods should be used to improve outcomes after cardiac surgery. One of them, is the choice of anaesthetic technique. Objectives: To evaluate the effects of sevoflurane, isoflurane and propofol on blood oxygen transport function and body energy expenditure during cardiac surgery in adults. Materials and methods. A total of 90 patients were included in the study. All patients were divided into 3 groups: 1- (n=30) included patients who were anesthetized with propofol. The second group (n=30) consisted of patients who underwent sevoflurane inhalation anaesthesia. Group 3 (n=30) was treated with isoflurane. All patients underwent coronary artery bypass grafting under cardiopulmonary bypass.
NCT05695287 ↗ The Effects of Sevoflurane, Isoflurane and Propofol During Cardiac Surgery Completed Astana Medical University Phase 1 2021-01-22 Abstract Anaesthetic support for cardiac surgery significantly influences the course of the intraoperative period and the success of the postoperative period. Total intravenous anaesthesia and inhalation anaesthesia are the traditional methods of anaesthesia in cardiac surgery. However, there are few studies assessing the effectiveness of surgical aggression protection in cardiac surgery. Objectives: To study the effectiveness of body protection against surgical aggression by TIVA and inhalational anaesthesia in cardiac surgery. Materials and methods. The examination and treatment data of 89 patients were included in the study. All patients underwent coronary artery bypass grafting, mitral valve replacement/plasty, aortic valve replacement cardiopulmonary bypass conditions. The patients were divided into 2 groups according to the type of disease: the first (1) group with coronary heart disease. The second (2) group with valvular heart disease. There were 65 patients in the first group and 22 in the second. Both groups were divided into 3 subgroups according to the type of anaesthesia: patients anaesthetised with propofol, with sevoflurane, with isoflurane.
NCT05742789 ↗ Effect of Anesthetics on Cardiac Biomarkers in Mitral and Aortic Valve Replacement/Plasty Completed Astana Medical University Phase 1 2021-11-30 Abstract Cardiac troponin is one of the biomarkers of the heart, and its high level correlates with a high risk of damage to cardiomyocytes. Objective: To determine the effect of anesthetics on cardiac enzymes during mitral and aortic valve replacement in adults. methods. Single-center prospective randomized controlled clinical study. A total of 255 patients were assigned randomly into three groups according to the type of anesthesia: the first group of 85 patients with propofol, the second group with sevoflurane - 85 patients, and the last - 85 patients were with isoflurane. Cardiac troponin I levels were calculated in ng/mL using the i-CHROMAII portable fluorescent analyzer manufactured by BoditechMedInc. (South Korea). Normal range:
NCT07044180 ↗ Reversal of Pipecuronium-induced Neuromuscular Blockade With Sugammadex During Propofol Anesthesia ACTIVE_NOT_RECRUITING Tamas Vegh, MD PHASE4 2025-06-26 Safety during modern practice of anaesthesia is of great concern. Patients admitted daily for surgical procedures undergoing general anaesthesia for different types of operations are exposed to different risks, starting from the anaesthesia and ending with the surgical intervention. Aim of the study is to provide a comprehensive and evidence based data regarding the safety of the neuromuscular blocking agents used in modern anaesthesia practice, precisely Rocuronium and Pipecuronium, as well as the reversal agents such as Sugammadex, which is the sole agent in use in practice nowadays. A routine anaesthetic practice will be performed during the whole period of our study after strict patient selection criteria. Intraoperative standard monitoring as per local and international guidelines will be applied, this includes Spo2, ECG, NIBP/IBP, etCO2, BIS and Tetragaph for neuromuscular blockade monitoring. After induction of anaesthesia and prior to the administration of the muscle relaxant agent, a TOFC (Train of Four Count) will be registered as the starting point. Throughout the anaesthetic time, there will be continuous TOF monitoring. The anaesthesia will be maintained by sevoflurane. Also, the recruited samples will be divided according to the neuromuscular blockade agents administered, either Rocuronium or Pipecuronium. At the end of the surgical procedure, the time lapse between the administration of the reversal agent Sugammadex and a TOF ratio of 0.9 is registered as our primary end point. TOF measures will be performed in the postoperative period, to make sure there is no residual neuromuscular blockade in the early postoperative phase. The study will not only monitor the safety of the neuromuscular blocking agents in use, but will also monitor any signs of anaphylaxis due to their administration both intra and postoperatively.
NCT07044193 ↗ Reversal of Pipecuronium-induced Neuromuscular Blockade With Sugammadex During Sevoflurane Anesthesia NOT_YET_RECRUITING Tamas Vegh, MD PHASE4 2025-06-26 Safety during modern practice of anaesthesia is of great concern. Patients admitted daily for surgical procedures undergoing general anaesthesia for different types of operations are exposed to different risks, starting from the anaesthesia and ending with the surgical intervention. Aim of the study is to provide a comprehensive and evidence based data regarding the safety of the neuromuscular blocking agents used in modern anaesthesia practice, precisely Rocuronium and Pipecuronium, as well as the reversal agents such as Sugammadex, which is the sole agent in use in practice nowadays. A routine anaesthetic practice will be performed during the whole period of our study after strict patient selection criteria. Intraoperative standard monitoring as per local and international guidelines will be applied, this includes Spo2, ECG, NIBP/IBP, etCO2, BIS and Tetragaph for neuromuscular blockade monitoring. After induction of anaesthesia and prior to the administration of the muscle relaxant agent, a TOFC (Train of Four Count) will be registered as the starting point. Throughout the anaesthetic time, there will be continuous TOF monitoring. The anaesthesia will be maintained by sevoflurane. Also, the recruited samples will be divided according to the neuromuscular blockade agents administered, either Rocuronium or Pipecuronium. At the end of the surgical procedure, the time lapse between the administration of the reversal agent Sugammadex and a TOF ratio of 0.9 is registered as our primary end point. TOF measures will be performed in the postoperative period, to make sure there is no residual neuromuscular blockade in the early postoperative phase. The study will not only monitor the safety of the neuromuscular blocking agents in use, but will also monitor any signs of anaphylaxis due to their administration both intra and postoperatively.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for pipecuronium bromide

Condition Name

Condition Name for pipecuronium bromide
Intervention Trials
Mitral Valve Insufficiency 2
Neuromuscular Blocking Agents 2
Residual Neuromuscular Block 2
Reversal of Neuromuscular Blockade 2
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Condition MeSH

Condition MeSH for pipecuronium bromide
Intervention Trials
Heart Diseases 2
Coronary Artery Disease 2
Delayed Emergence from Anesthesia 2
Mitral Valve Insufficiency 2
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Clinical Trial Locations for pipecuronium bromide

Trials by Country

Trials by Country for pipecuronium bromide
Location Trials
Kazakhstan 3
Hungary 2
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Clinical Trial Progress for pipecuronium bromide

Clinical Trial Phase

Clinical Trial Phase for pipecuronium bromide
Clinical Trial Phase Trials
PHASE4 2
Phase 1 2
N/A 1
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Clinical Trial Status

Clinical Trial Status for pipecuronium bromide
Clinical Trial Phase Trials
Completed 3
NOT_YET_RECRUITING 1
ACTIVE_NOT_RECRUITING 1
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Clinical Trial Sponsors for pipecuronium bromide

Sponsor Name

Sponsor Name for pipecuronium bromide
Sponsor Trials
Astana Medical University 3
Tamas Vegh, MD 2
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Sponsor Type

Sponsor Type for pipecuronium bromide
Sponsor Trials
Other 5
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