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Preanesthetic Medication clinical trials

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NCT ID: NCT04273035 Recruiting - Tonsillectomy Clinical Trials

Handheld-multimedia Versus Oral Midazolam in Pediatric on Perioperative Anxiety

Start date: February 1, 2020
Phase: Phase 4
Study type: Interventional

The first goal of this study is to compare the efficacy and safety between anxiolysis by multimedia-distraction with an IPAD versus anxiolysis by premedication with midazolam prior to the induction. Secondly to evaluate the need for midazolam-premedication in pediatric day-care patients induced by inhalational anesthesia.

NCT ID: NCT03931057 Completed - Clinical trials for Preanesthetic Medication

The Use of ADV6209 for Premedication in Pediatric Anesthesia

Start date: November 16, 2020
Phase: Phase 4
Study type: Interventional

To evaluate the effect of ADV6209, a new oral Midazolam formulation, on preoperative anxiety and sedation levels in paediatric anaesthesia Primary Objective: Sedation score (mYPAS) 30 min after administration of the premedication drug Secondary Objective: Acceptance of anaesthesia mask induction Acceptance of oral administration of the premedication drug

NCT ID: NCT03474939 Completed - Clinical trials for Preanesthetic Medication

The Effect of Midazolam Premedication on Copeptine Concentration in Blood

Start date: April 3, 2017
Phase: Phase 4
Study type: Interventional

The study aim is to assess whether premedication with midazolam prior to surgery affects copeptin concentration in blood.

NCT ID: NCT03052660 Completed - Clinical trials for Preanesthetic Medication

Impact of Preoperative Midazolam on Outcome of Elderly Patients

I-PROMOTE
Start date: October 12, 2017
Phase: Phase 4
Study type: Interventional

We aim to assess, if placebo compared to preoperative administration of midazolam in elderly patients is equal in regard to the global postoperative patient satisfaction

NCT ID: NCT01937611 Recruiting - Laryngoscopy Clinical Trials

Intramuscular Dexmedetomidine as Premedication

Start date: March 2013
Phase: Phase 4
Study type: Interventional

Many studies have been conducted for the feasibility of using dexmedetomidine as premedication. However, bradycardia and hypotension frequently occurred following the premedication with dexmedetomidine, either via intramuscular or intravenous route. This is particularly true when using a high dose of dexmedetomidine: a intramuscular dose over 2 μg•kg-1 or a intravenous dose over 1 μg•kg-1 can elicit marked decreases in heart rate and mean arterial blood pressure. Subsequent studies using high-dose dexmedetomidine further revealed the potential impact of its detrimental haemodynamic profile on clinical outcomes. Most studies using high-dose dexmedetomidine were predominantly adopted with the dose-finding study performed by Aho and colleague, whom reported that 2.5 μg•kg-1 dose of intramuscular dexmedetomidine was comparably sedative and anxiolytic to 0.08 mg•kg-1 midazolam. However, few investigations have addressed the clinical effects of low-dose dexmedetomidine as premedication. Considering modern anaesthesia has advanced a long way towards eliminating the routine need for a deep preoperative sedation. It has, therefore, become desirable to asses dexmedetomidine as an effective premedication using a moderate sedative dose to minimize its undesired hemodynamic effects. We set a prospective study to compare the sedative, haemodynamic, adjuvant anaesthetic effects and patient's satisfaction of low-dose dexmedetomidine (1μg•kg-1) with midazolam (0.03 mg•kg-1), the most commonly used premedication, used as an intramuscular injective administration in patients undergoing suspension laryngoscopic surgery under general anaesthesia.