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Unconsciousness clinical trials

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NCT ID: NCT04581642 Completed - Pain Clinical Trials

Nociception-Level (NOL) for the Assessment of Pain in Patient Unable to Self-Report

MoNOLog
Start date: November 1, 2020
Phase:
Study type: Observational

In this study we aimed to investigate the performance and effectiveness of NOL and/or NOLedge as a tool for pain assessment in geriatric and critical ill non communicating patients. Our hypothesis was that NOL and the NOLedge may have good correlation with the health-care professional assessment PAINAD, BPS values, even with the use of the drugs affecting autonomic nervous system.

NCT ID: NCT04315389 Completed - Stroke Clinical Trials

SG Healthcare and Assistive Robotics Programme (SHARP) - Proof of Concept Study

SHARPCARE
Start date: December 2, 2020
Phase:
Study type: Observational

Robots are commonly used in many settings to help with transportation needs, reduce human injuries, and assisting clinicians during surgeries. These applications could provide direct benefits to patients in the clinical rehabilitation field. In this study, the feasibility of 2 CARE robot prototypes in facilitating dependent transfers and assisting patient mobility in their daily living activities will be studied.

NCT ID: NCT04306601 Completed - Clinical trials for Traumatic Brain Injury With Prolonged Loss of Consciousness

Low-Intensity Focused Ultrasound on Individuals With Disorder of Consciousness of Traumatic Brain Injury

Start date: June 25, 2020
Phase: N/A
Study type: Interventional

Low-intensity focused ultrasound can be effective in severe TBI patients with disorder of consciousness. This study is a prospective single arm, open-label and explorative clinical trial to evaluate the therapeutic effect of recovery from DoC and safety of low-intensity focused ultrasound stimulation at thalamic area in patients with post-traumatic DoC.

NCT ID: NCT04000126 Completed - Pain Clinical Trials

Pupillometry - Future of Objective Pain Reaction Measurement While Unconscious

Start date: February 25, 2019
Phase: N/A
Study type: Interventional

This study aims to assess the usefulness of pupillometry as a nociceptive indicator during elective orotracheal intubation in patients given intravenous lignocaine pre-intubation as compared to a placebo pre-intubation.

NCT ID: NCT03998930 Completed - Stroke Clinical Trials

Evaluation of Consciousness by Brain-computer Interface in Severely Brain Damaged Patients

AWAKE
Start date: March 6, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to show that the measurement of auditory and vibro-tactile evoked potentials, or the recording of the EEG signal during a motor imaging task, can be used in routine clinical situations to explore the state of consciousness of subjects in Non-responsive Awakening (or Chronic Vegetative State) or in Minimal Consciousness (or relational state) after a severe brain injury. Assumptions : - Correlation between patient response rates obtained with the brain-machine interface and their clinical consciousness score (Coma Recovery Scale Revised score) - Differentiation of the parameters of the evoked potentials P300 between patients in a vegetative state and those in a state of minimal consciousness

NCT ID: NCT03913065 Completed - Computed Tomography Clinical Trials

Head Computed Tomography for Predicting Neurological Outcome After Cardiac Arrest

Start date: November 18, 2017
Phase:
Study type: Observational [Patient Registry]

The European Resuscitation Council (ERC) and the European Society of Intensive Care Medicine (ESICM) joint guidelines for post-resuscitation care recommend a multimodal approach to prognostication of neurological outcome. However, head computed tomography (CT) which is commonly used for predicting long-term neurological outcome after cardiac arrest has not yet been examined prospectively in a clinical trial. The primary purpose of the TTM-2 CT-substudy is to prospectively investigate and compare various methods of diagnosing generalized oedema on CT after cardiac arrest and it´s ability to predict long-term neurological outcome.

NCT ID: NCT03858400 Completed - Conditions of Brain Clinical Trials

Electrophysiological Tests on Unconscious Patient

Start date: March 20, 2017
Phase:
Study type: Observational [Patient Registry]

Most patients with minimal consciousness status in Critical Care Units (CCU) are considered as an 'unconscious patient' with a neurological examination. Evaluating these patients as unconscious patients may lead to neglect of psychosocial needs in patient-care, a continuation of unchanged treatment protocols for a long time and desperate evaluation of prognosis. In this study, the investigators aimed to evaluate the emotional responses of patients who were considered by the healthcare providers and relatives of patients as an 'unconscious patient' by using electrophysiological tests.

NCT ID: NCT03727464 Completed - Clinical trials for Unconscious (Psychology)

Memory Priming in General Anesthesia

Start date: January 7, 2013
Phase: N/A
Study type: Interventional

Memory priming under general anesthesia is a phenomenon of incredible interest in the study of consciousness and unconscious cognitive processing, and for clinical practice. However results from anesthesiological literature are divergent and methodologies vary. To overcome these limits, the present study aims at better defining the phenomenon of memory priming under general anesthesia, manipulating as experimental variables both the anesthetic drug used and the stimuli primed.

NCT ID: NCT03699306 Completed - Unconsciousness Clinical Trials

Comparison of Three Methods for NG Tube Placement

NG
Start date: January 21, 2017
Phase: N/A
Study type: Interventional

Background and Aim: Tubular feeding is used, in patients who cannot take food through their mouths, but the digestive system has the ability to digest food. This method is safe and affordable for the patient and results in maintaining the function of the digestive system and reducing the risk of infection and sepsis. The purpose of this study was to compare the three methods of the NG tube placement in intubated patients in the emergency department of university-affiliated hospitals of Isfahan from2016 to 2018. Materials and Methods: This study was a randomized and prospective clinical trial. The statistical population of this study was all patients who had been referred to the emergency department of Al-Zahra and Ayatollah Kashani hospitals in Isfahan between2016and2018. The sample size was 25 in each group, and in total 75 subjects. The first group was NG tube insertion by the conventional method, the second group was using brake cable and the third group was embeddedby highwayman's hitch or draw hitch, using a silk thread. For all patients, demographic characteristics and possible complications were recorded. Finally, the data were analyzed using SPSS20 software at two statistical levels of descriptive and inferential.

NCT ID: NCT03605979 Completed - Type 1 Diabetes Clinical Trials

Continuous Glucose Monitoring and Hypoglycemia Unawareness in Type 1 Diabetes

Start date: July 1, 2012
Phase:
Study type: Observational

Looking for strict normoglycemia in type 1 diabetes increases the risk of hypoglycemia, exposing to hypoglycemia unawareness. It has been shown that the early correction of hypoglycemia can help recovering the perception of hypoglycemia. The purpose of this prospective study was to assess the value of sensor-augmented insulin-pump therapy to treat hypoglycemia unawareness.