Clinical Trials Logo

Anesthesia clinical trials

View clinical trials related to Anesthesia.

Filter by:

NCT ID: NCT02571426 Completed - Anesthesia Clinical Trials

Renal Function During Pediatric Anesthesia

Start date: October 2015
Phase: Phase 1
Study type: Interventional

It is known that volatile anesthesia, such as sevoflurane, retain water and that this appears more pronounced in children. However, the mechanisms for this effect is unknown and it is not clear if the commonly used anesthetic propofol does the same. In this study the investigators want to compare the fluid and electrolyte conserving effects of sevoflurane and propofol in a pediatric setting and also investigate humoral changes induced by these anesthetics.

NCT ID: NCT02567968 Completed - Anesthesia Clinical Trials

A Study to Determine if Caffeine Accelerates Emergence From Anesthesia

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

At present clinicians have no way to reverse anesthesia. Patients wake when their bodies clear the anesthetic. Most people wake quickly, but some do not. All patients have memory and other cognitive problems after waking from anesthesia. In studies on animals, the investigators observed that caffeine caused rats and mice to wake much more rapidly from anesthesia. This was true for all the animals tested. The investigators would like to see if this holds true in humans. Will caffeine accelerate waking from anesthesia? Will it reverse the cognitive deficits associated with anesthesia, after waking? The investigators carried out a modest trial with 8 test subjects. Each volunteer was anesthetized twice. Each volunteer was anesthetized one time and received an infusion of saline (placebo control), without the aid of any other drugs and the other time the volunteer received an infusion of a relatively low dose of caffeine. The order of saline versus caffeine was randomized and the study was done in a double blind manner. We observed that emergence from anesthesia was significantly accelerated by the caffeine infusion. No adverse events were observed.

NCT ID: NCT02563795 Completed - Anesthesia Clinical Trials

Low Dose Spinal Anesthesia in Cesarean Surgery

Start date: May 2015
Phase: N/A
Study type: Observational [Patient Registry]

Anesthesia for cesarean section requires special importance because it may affect both mother and the baby. To avoid maternal hypotension related to spinal anesthesia must be the primary objective during anesthesia. Even though many factors influence sensory nerve block for surgical anesthesia, local anesthetic dose is the main determinant. Another factor that influence the sensory nerve block is the obesity related to pregnancy. Due to the enlargement of epidural venous plexus related to pregnancy, the subarachnoid and epidural space reduces, so the local anesthetic requirement also reduces. Many investigators recommend lower dose of local anesthetic in obese patients due to reduced requirement There are many studies about dose regimens for cesarean anesthesia, but ideal dose have not been found. Investigators have designed this study to see the effects of conventional dose (10 mg bupivacaine) vs. low dose plus fentanyl (7,5 mg bupivacaine+25 mcg fentanyl) in obese and normal weight pregnant for cesarean section. The hypothesis was: the low dose regimen provides surgical anesthesia in obese patients while avoiding maternal hypotension.

NCT ID: NCT02555046 Not yet recruiting - Anesthesia Clinical Trials

Muscle and Cerebral Oxygenation Under EVAR of AAA: GA vs LA

Start date: October 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of General versus Local Anaesthesia on muscle and cerebral oxygenation under EVAR-treatment in a prospective unblinded randomised controlled trail.

NCT ID: NCT02554864 Completed - Anesthesia Clinical Trials

Location of Injection of Local Anesthetics in the Adductor Canal Block

LILAC
Start date: February 22, 2016
Phase: N/A
Study type: Interventional

The adductor canal block (ACB) is the standard of care for analgesia after Anterior Cruciate Ligament (ACL) repair. ACB is performed by injecting local anesthetic (freezing) in the subsartorial canal in the thigh which is about 7-10cm long. Preliminary evidence suggests that different injection sites within the canal may produce different degrees of analgesia and quadriceps motor block. This trial seeks to determine the effects of various ACB injection sites on postoperative analgesia and motor power following ACL repair.

NCT ID: NCT02550587 Active, not recruiting - Anesthesia Clinical Trials

Patient Satisfaction With Anesthesia Care

Start date: September 2015
Phase: N/A
Study type: Observational

The level of patient satisfaction is an important indicator of health care quality because it causes to reconsider the functioning of the hospital and go to the new regulations. Postoperative thought gives us important information for improving the quality of anesthesia care and health care quality. The investigators aimed to investigate the status of the anesthesia satisfaction in patients.

NCT ID: NCT02544854 Recruiting - Anesthesia Clinical Trials

Pharmacokinetic/Pharmacodynamic Model of Propofol in Children

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

By measuring plasmatic concentration of propofol at different intervals during surgery of children aged 1 to 12 years old and measuring Bispectral Index (BIS) as a surrogate for cerebral activity, the investigators aim to create a pharmacokinetic/pharmacodynamic model of propofol for children.

NCT ID: NCT02536690 Completed - Anesthesia Clinical Trials

Remifentanil and Midazolam on Propofol for Loss of Consciousness

Start date: August 2015
Phase: N/A
Study type: Interventional

Propofol in combination with remifentanil or midazolam can result in synergistic or additive effect. The patients who are scheduled to undergo general anesthesia are enrolled in this study. 120 patients will be randomly allocated to 3 groups(P, PR, PMR). The patients in group P will receive general anesthesia only with propofol and group PR and PMR will receive 0.25 mcg/kg/min remifentanil infusion prior to propofol. The patients in group PMR will receive 0.03 mg/kg bolus dose of midazolam 1 min after start of the remifentanil infusion. 'Success' is defined as loss of both verbal response and eyelash reflex in 2 min after propofol administration. When 'success', the next patient will receive the same dose(in 18/19 probability) or 0.25 mg/kg lower dose(in 1/19 probability) of propofol. When 'failure', the next patient will receive 0.25 mg/kg higher dose of propofol at induction period.

NCT ID: NCT02534285 Completed - Anesthesia Clinical Trials

the Impact of Noise on Requirements of Anesthetics During General Anesthesia

Start date: August 2015
Phase: N/A
Study type: Interventional

The investigators hypothesize that the noise level in the operating theatre influences the patients' requirements of anesthetics. Study subject are patients undergoing abdominal surgery in combined general and epidural anesthesia. Analgesia is maintained by epidural injections of sufentanil and ropivacaine whereas general anesthesia is maintained using the inhalational anesthetic desflurane. Desflurane requirements are adjusted using neuromonitoring (BIS-Index). Intraoperative noise levels are recorded. Patients are randomized to receive hearing protections or not.

NCT ID: NCT02531477 Recruiting - Anesthesia Clinical Trials

Intra-carotid Anesthetic Agent Delivery

ICAAD
Start date: January 2015
Phase: N/A
Study type: Interventional

Intra-Carotid delivery of propofol.