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Neuromuscular Blockade clinical trials

View clinical trials related to Neuromuscular Blockade.

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NCT ID: NCT02822001 Recruiting - Clinical trials for Respiratory Insufficiency

Sugammadex vs. Placebo to Prevent Residual Neuromuscular Block in the Post--‐Anesthesia Care Unit

Sugammadex
Start date: February 16, 2017
Phase: Phase 4
Study type: Interventional

The Primary objective of this study is to determine whether patients who receive sugammadex immediately after tracheal extubation will exhibit a decrease in the incidence of postoperative residual paralysis and an associated decrease in the incidence of postoperative respiratory depression (which can precede critical respiratory events, CRE). The Secondary objectives are to: a) determine whether patients receiving sugammadex will have a normal TOF ratio (>0.90) indicative of full neuromuscular recovery in the PACU; and b) to improve patient safety by documenting whether postoperative respiratory depression (decreased MV below 80% and 40% of predicted MV as assessed by a Respiratory Volume Monitor) is due to opioid administration vs. postoperative residual neuromuscular block (by comparing postoperative VAS scores and total opioid administered).

NCT ID: NCT02794714 Withdrawn - Clinical trials for Neuromuscular Blockade

Deep vs Moderate Block: Impact on Operating Conditions & Patient Satisfaction

Start date: June 2016
Phase: Phase 4
Study type: Interventional

This study compares surgeon's satisfaction of operating conditions and patient's satisfaction following laparoscopic gynecological surgeries in two groups of patients, half of whom will receive deep neuromuscular blockade and the other half, moderate neuromuscular blockade.

NCT ID: NCT02724111 Completed - Surgery Clinical Trials

Effect of Neuromuscular Blockade on Operating Conditions and Overall Satisfaction During Spinal Surgery

Start date: May 15, 2016
Phase: Phase 4
Study type: Interventional

The investigators aim to investigate operating conditions, postoperative recovery and overall satisfaction of surgeons between deep neuromuscular blockade (NMB) group and restricted NMB group during spinal surgery under general anesthesia. The investigators hypothesize that this study can present good surgical conditions, postoperative recovery outcomes and overall satisfaction of surgeons in deep NMB group, thereby proving the advantages of deep NMB as well as flaws of restricted NMB in spine surgeries.

NCT ID: NCT02709473 Completed - Anesthesia Clinical Trials

The Effect of Propofol and Remifentanil Sequence on ED50 and ED95 of Rocuronium in Rapid Sequence Induction Anesthesia

Start date: March 2016
Phase: Phase 4
Study type: Interventional

Rapid sequence induction (RSI) is a well-known procedure to maintain a safe and rapid airway in patients especially at risk of aspiration. Propofol and rocuronium are generally used agents for RSI. However, the difficult airway scenarios are always valid for these patients, even without predictive signs of difficult airway. Therefore, it is important to decrease the rocuronium dose used in RSI to achieve a rapid recovery of a neuromuscular conduction with the aid of a reversal agent in case of difficult airway. The short acting opioids such as remifentanil may be helpful to reduce the dose of rocuronium in RSI.

NCT ID: NCT02635542 Completed - Clinical trials for Postoperative Complications

Effect of Neuromuscular Blockade on Pulmonary Complications in Elective Cardiac Surgery

Start date: March 2016
Phase: Phase 4
Study type: Interventional

The investigators will conduct a prospective, randomized trial to assess the impact of neuromuscular blockade on early (<72 hours post-ICU admission) postoperative respiratory complications in cardiac surgical patients. The study will compare continual neuromuscular blockade with cisatracurium to a single dose of succinylcholine during general anesthesia for cardiac surgery.

NCT ID: NCT02601508 Not yet recruiting - Clinical trials for Neuromuscular Blockade

Compare of Surgical Condition and Complications With Moderate and Deep NM Block

MISPCNUHH
Start date: November 2015
Phase: N/A
Study type: Interventional

This study is designed to evaluate the surgeon's satisfaction with either deep or moderate neuromuscular blockade during laparoscopic gastrectomy surgery and observe the recovery profiles in the recovery room and the ward.The explorative objective of this study is to evaluate the safety profiles of deep and moderate neuromuscular blockades via observation of postoperative complications.

NCT ID: NCT02580188 Completed - Clinical trials for Neuromuscular Blockade

The Effect of Deep Neuromuscular Block on Surgical Condition During Laparoscopic Colorectal Surgery

DEEPCOL
Start date: March 24, 2015
Phase: Phase 4
Study type: Interventional

This study is a randomized, controlled, double-blinded, and parallel design study. A total 96 patients were randomized to receive a deep block or a moderate block scheduled for elective laparoscopic colorectal surgery. Investigators estimated the proportion of intra-abdominal pressure(IAP) alarm and surgical rating score.

NCT ID: NCT02562417 Withdrawn - Clinical trials for Neuromuscular Blockade

Impact of iv Dexamethasone on Reversal of Rocuronium-induced Neuromuscular Block by Sugammadex

Start date: June 2016
Phase: Phase 4
Study type: Interventional

Sugammadex is used as a reversal drug for rocuronium- or vecuronium-induced neuromuscular block during general anaesthesia. IV dexamethasone is injected as a prophylactic measure against postoperative nausea and vomiting. Recent animal data have shown that dexamethasone may impair the reversal effect of sugammadex. The objective of this randomised controlled trial is to confirm in the clinical practice these preliminary results.

NCT ID: NCT02546843 Completed - Clinical trials for Neuromuscular Blockade

Depth of Neuromuscular Blockade and the Perioperative Conditions in Laparoscopic Surgery in Pediatric Population

PedLapBlock
Start date: December 2015
Phase: N/A
Study type: Interventional

This randomized study prospectively evaluates our experience with administration of cisatracurium and rocuronium antagonized by sugammadex and evaluates the effects of various depths of neuromuscular blockage on providing optimal surgical conditions during laparoscopy with low-pressure capnoperitoneum.

NCT ID: NCT02513693 Recruiting - Clinical trials for Neuromuscular Blockade

Deep Neuromuscular Blockade During Robotic Radical Prostatectomy

Start date: July 2015
Phase: Phase 4
Study type: Interventional

Basic requirement for safe performance of the robotic intra-abdominal surgery is a calm and clear surgical field after the introduction of a capnoperitoneum. That can be enabled by a neuromuscular blockade. Provision of standard neuromuscular blockade is a compromise between optimal surgical conditions (sufficiently deep block) and capability to antagonize the block rapidly at the end of the surgery. With rocuronium, it is possible to maintain deep neuromuscular blockade safely until the very end of the surgery, and unlike with spontaneous recovery or reversal of the block with neostigmine, administration of sugammadex at the end of the surgery will enable quick and consistent reversal of the block. Project is focused on comparison of the parameters of deep and standard neuromuscular blockade - surgical conditions (primary endpoint), quality of recovery and turnover time (secondary endpoints).