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Last Updated: October 20, 2019

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CLINICAL TRIALS PROFILE FOR VECURONIUM BROMIDE

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Clinical Trials for Vecuronium Bromide

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00970762 Comparative Study of Rocuronium With Vecuronium (Study 71101)(COMPLETED) Completed Merck Sharp & Dohme Corp. Phase 3 2003-02-01 This study was conducted to determine and compare the safety and effectiveness of two neuromuscular blockers (rocuronium and vecuronium) at various doses in adults who are undergoing general elective surgery with sevoflurane anesthesia. Study participants received an intubating dose of a neuromuscular blocker (to enable insertion of a tube through the nose or mouth into the trachea to provide artificial ventilation). The intubating dose was followed by repeated bolus maintenance doses as needed, to maintain muscle relaxation. The time it takes to reach maximal effect of the neuromuscular blocker (onset time) after the intubating dose was measured and compared as the primary outcome.
NCT01116713 Effect of Dexamethasone in Postoperative Symptoms After Mastectomy for Breast Cancer Completed Instituto Mexicano del Seguro Social Phase 3 2009-06-01 Postoperative pain, nausea and vomiting (PONV) are the most common complications after anesthesia and surgery. Women undergoing mastectomy with axillary dissection are at a particularly high risk for the development of PONV and an incidence of 60-80% in patients receiving no antiemetic has been reported. Emetic episodes predispose to aspiration of gastric contents, wound dehiscence, psychological distress, and delayed recovery and discharge times. These justify the use of prophylactic antiemetics in women scheduled for mastectomy. Most of the currently used antiemetics, including antihistamines, butyrophenones and dopamine receptor antagonists have been reported to cause occasional undesirable adverse effects, such as excessive sedation, hypotension, dry mouth, dysphoria, hallucinations and extrapyramidal signs. Antiserotonins (e.g., ondansetron) are available for the prevention and treatment of PONV in patients undergoing various types of surgery [4]. However, the use of prophylactic antiemetic therapy with antiserotonins has been criticized for being too expensive. Dexamethasone was first reported to be an effective antiemetic regimen in patients receiving cancer chemotherapy. The purpose of this study was to evaluate the efficacy of dexamethasone treatment for reducing pain and PONV as well as analgesic and antiemetic requirements in women undergoing general anesthesia for mastectomy with axillary lymph node dissection.
NCT02599168 Effect of Dexmedetomidine on Propofol Requirement During Anesthesia Recruiting Dr Nitin Sethi Phase 4 2015-12-01 Dexmedetomidine, a selective alpha-2 agonist agent used for maintaining sedation in intensive care patients in receipt of mechanical ventilation, is being increasingly utilized in anaesthesia practice for facilitating anaesthesia depth as an adjunct to base anaesthetics (intravenous; propofol: inhalational; sevoflurane, desflurane). The investigators intend to assess the anaesthetic potential of dexmedetomidine in controlled anaesthesia settings empowered by the use of an objective, patient response based, safe, efficient, and patented closed loop anaesthesia delivery system (CLADS). CLADS functions on control of processed EEG response parameter captured from anaesthetized patients with the help of a BIS- monitor, which is continuously fed into a automated drug infusion pump. The infusion pump then accordingly delivers the anaesthetic drug to the patients based on pharmacodynamic requirements. If dexmedetomidine has anaesthesia potential then it is likely that propofol use delivered by CLADS can be reduced further. In addition the effect of two drugs (viz, base agent-propofol plus adjunct agent-dexmedetomidine) on different receptor site within the brain would help gain greater anaesthetic depth consistency as well as a lower incidence of intraoperative patient awareness. This prospective randomized two-arm study aims to assess effect of the use of dexmedetomidine on propofol requirements (primary objective), anaesthesia depth consistency, and intraoperative patient awareness (secondary objectives).
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Vecuronium Bromide

Condition Name

Condition Name for Vecuronium Bromide
Intervention Trials
Anesthesia 3
Postoperative Vomiting 1
Hepatic Metastases 1
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Condition MeSH

Condition MeSH for Vecuronium Bromide
Intervention Trials
Vomiting 1
Hepatoblastoma 1
Postoperative Nausea and Vomiting 1
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Clinical Trial Locations for Vecuronium Bromide

Trials by Country

Trials by Country for Vecuronium Bromide
Location Trials
India 2
United States 1
Mexico 1
Russian Federation 1
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Trials by US State

Trials by US State for Vecuronium Bromide
Location Trials
Maine 1
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Clinical Trial Progress for Vecuronium Bromide

Clinical Trial Phase

Clinical Trial Phase for Vecuronium Bromide
Clinical Trial Phase Trials
Phase 4 5
Phase 3 2
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Vecuronium Bromide
Clinical Trial Phase Trials
Not yet recruiting 4
Completed 3
Recruiting 2
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Clinical Trial Sponsors for Vecuronium Bromide

Sponsor Name

Sponsor Name for Vecuronium Bromide
Sponsor Trials
Merck Sharp & Dohme Corp. 3
Postgraduate Institute of Medical Education and Research 2
Maine Medical Center 1
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Sponsor Type

Sponsor Type for Vecuronium Bromide
Sponsor Trials
Other 8
Industry 3
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