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Anesthesia clinical trials

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NCT ID: NCT03231683 Completed - Anesthesia Clinical Trials

Use of S+Ketamine During Target-Controlled Intravenous Anaesthesia After Abdominal Hysterectomy

Start date: March 2014
Phase: Phase 2
Study type: Interventional

The investigators want to investigate the effect of low dose S+ ketamine compared to placebo on cumulative morphine consumption at 24 hours in 90 women undergoing open abdominal hysterectomy with remifentanil-propofol target controlled infusion (TCI) in KK Women's and Children's Hospital. The secondary aims are to investigate the use of low dose S+ ketamine on the incidence of nausea, vomiting, pruritus (opioid side effect), sedation score and psycho mimetic assessment compared to placebo group. The investigators propose to conduct a double blinded, randomized controlled study in women undergoing open abdominal hysterectomy with remifentanil-propofol TCI. (1) Treatment Group: intravenous ketamine 0.5 mg/kg at the beginning and 0.5 mg/kg 20 minutes before extubation. (2) Control Group: intravenous normal saline (as placebo) at the beginning and 20 minutes before extubation.

NCT ID: NCT03229148 Completed - Stroke Clinical Trials

Anesthesia Management in Endovascular Therapy for Ischemic Stroke

AMETIS
Start date: August 31, 2017
Phase: N/A
Study type: Interventional

Objective of the study: to assess whether pharmacological sedation or general anesthesia for treatment of anterior circulation ischemic stroke with endovascular mechanical thrombectomy is associated with difference in morbidity (neurological outcome and peri-procedural complications).

NCT ID: NCT03218306 Recruiting - Pain Clinical Trials

Surgical Pleth Index (SPI) Versus Standard Clinical Approach Analgesia

SPIDER
Start date: October 23, 2017
Phase: N/A
Study type: Interventional

The study is aimed at confronting a surgical pleth index based protocol for intraoperative analgesia in a desflurane based general anesthesia for thyroidectomy, versus a standard clinical approach. A reduction in analgesic consumption and improvement in hemodynamics are expected.

NCT ID: NCT03218124 Not yet recruiting - Anesthesia Clinical Trials

Optimal Remifentanil Concentration and Thyroidectomy

ORCO
Start date: October 1, 2017
Phase: N/A
Study type: Interventional

The study is aimed at determining the remifentanil effect site concentration suppressing the cough at extubation after surgical thyroidectomy, performed under remifentanil/desflurane based general anesthesia, expressed as median and 95th percentile effective dose. Possible hemodynamic instability, respiratory depression or prolongation of awakening time are also sought.

NCT ID: NCT03214497 Completed - Anesthesia Clinical Trials

Protectorâ„¢ Versus Supreme® Laryngeal Mask Airway

Start date: July 12, 2017
Phase: N/A
Study type: Interventional

The goal of this study is to compare the oropharyngeal leak pressure of the Protector Laryngeal mask with the Supreme laryngeal mask. Other secondary parameters will be studied.

NCT ID: NCT03211949 Completed - Surgery Clinical Trials

Ultrasound Guided Topographic Mapping of Medial Antebrachial Cutaneous Nerve

Start date: September 2014
Phase: N/A
Study type: Interventional

Blocking the medial antebrachial cutaneous nerve (MACN) during an axillary block often a subcutaneous wheal of local anesthetics is made what is described as painful. With the improvement of the resolution of the ultrasound machines smaller structures and nerves can be visable. In this study topographic assessment will made of the anatomical variation of the medial antebrachial cutaneous nerve (MACN) by ultrasound in the axilla and 5 cm above the cubital fossa of the arm.

NCT ID: NCT03205189 Recruiting - Postoperative Pain Clinical Trials

Comparison Between Pre-operative Prescription Delivered During Anesthesia Consultation or Post-operative Prescription

AMBUPRESS
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

This study evaluates the comparison of the incidence of postoperative home pain after ambulatory surgery with general anesthesia between a group with pre-surgical prescription delivered during anesthesia preoperative clinic and a group with postoperative prescription.

NCT ID: NCT03195530 Terminated - Anesthesia Clinical Trials

Bispectral Index (BIS) Values Required for an Adequate Depth of Anesthesia in Elderly Patients Using Propofol

Start date: May 1, 2017
Phase:
Study type: Observational

A correlation between the bispectral index values and electroencephalographic patterns at the loss of consciousness (LOC) when using propofol in elderly patients, has not been determined. Our aim is to describe the BIS values and the power of the alpha band in the electroencephalography in elderly patients, at the LOC moment.

NCT ID: NCT03191838 Completed - Anesthesia Clinical Trials

Audiovisual Distraction for Patients Undergoing Total Knee or Hip Replacement Surgery

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

The primary purpose of this study is to investigate whether audiovisual distraction can lead to a reduction in standard of care administered intraoperative propofol consumption compared to those who receive propofol sedation alone in adults having total hip or knee replacement surgery under spinal anesthesia.

NCT ID: NCT03176680 Not yet recruiting - Anesthesia Clinical Trials

The Effects on Major Organ Complications on Esophagectomy of New Anesthetic ERAS Strategy: a Prospective Investigation

ERAS
Start date: June 15, 2017
Phase: N/A
Study type: Interventional

The goals of this study are to testify the effectiveness on enhancement recovery by new anesthetic ERAS (Enhanced recovery after surgery) strategy.