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Preoperative Anxiety clinical trials

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NCT ID: NCT03460145 Completed - Clinical trials for Preoperative Anxiety

Lavender Oil on Preoperative Anxiety and Sedation Requirement in General Anaesthesia

Start date: September 27, 2018
Phase: N/A
Study type: Interventional

Assessment of how Lavender oil reduces preoperative anxiety and subsequently influences requirement of induction agents for general anesthesia.

NCT ID: NCT03429179 Completed - Clinical trials for Preoperative Anxiety

Using Preoperative Anxiety Score to Determine the Precise Dose of Butorphanol for Sedation

Start date: March 5, 2018
Phase: Phase 2
Study type: Interventional

Pre-operative anxiety usually lead to increased anesthetics during the surgery. The precise sedative requirement which can keep adequate sedative state and avoid adverse effects caused by excessive drugs still needs further study. Therefore, our purpose was to confirm the sedative effect of butorphanol and to explore the relationship between pre-operative anxiety and intra-operative butorphanol requirement to evaluate the precise sedative requirement which can keep adequate sedation for patients by pre-operative anxiety score.

NCT ID: NCT02998801 Completed - Anxiety Clinical Trials

Alleviating Pre-operative Anxiety With Innovative 3D Immersive Virtual Reality

VR-Anxiety
Start date: November 2016
Phase: N/A
Study type: Interventional

To construct and evaluate an immersive 3D simulation to familiarize patients with the pre-operative experience, and investigate whether A) immersive 3D virtual reality video can reduce pre-operative anxiety, and B) how this approach compares to current practice of viewing traditional educational videos.

NCT ID: NCT02742025 Completed - Clinical trials for Preoperative Anxiety

Effect of an Educational and Explanatory Program for a Surgical Act on Preoperative Anxiety

HEART-LINK
Start date: November 19, 2019
Phase: N/A
Study type: Interventional

The main objective of this study is to evaluate the impact on preoperative anxiety of an education and information program conducted prior to non-urgent coronary angiography performed in patients hospitalized at the Nîmes University Hospital.

NCT ID: NCT02732197 Completed - Cesarean Section Clinical Trials

Effects of Sedation on Spinal Anesthesia-induced Maternal Hypotension

Start date: August 2014
Phase: N/A
Study type: Observational

Background: This study was designed to investigate the effect of sedation on the occurrence of maternal hypotension in preoperatively anxious parturients undergoing urgent category-1 Cesarean section (C/S) under spinal anesthesia. Methods: After institutional ethics committee approval, prospectively collected data of 1824 parturients undergoing C/S were reviewed. Parturients with high preoperative anxiety scores (visual analogue scale for anxiety (VAS-A)≥70) undergoing C/S under spinal anesthesia with thiopental (Group S=49) and without any other type of sedation (Group NS=53) were included in the analysis. Hemodynamic parameters were documented and maximum systolic arterial pressure (SAP) reductions from the baseline after spinal anesthesia were calculated. Incidences of hypotension (SAP≥30% decrease from baseline or <100 mmHg) and bradycardia (HR<55 beats/min), and related-ephedrine and -atropine requirements were noted. Our primary endpoint was to compare the maximum SAP reductions from the baseline values in Groups S and NS. Secondary endpoints were incidences of hypotension and bradycardia, required ephedrine and atropine doses, newborn Apgar scores at 1st and 5th min.

NCT ID: NCT02566642 Completed - Clinical trials for Preoperative Anxiety

Understanding the Role of the Anesthesiologist

Start date: October 2014
Phase: N/A
Study type: Observational

When presenting for elective surgery, patient's often do not completely understand the role that the anesthesiology team plays in their care. In 1999, the American Medical Association (AMA) found that health literacy was a stronger predictor of a person's health than age, income, education level and race. It is very important that the investigators provide information to patients on the role of anesthesiologists in their care before, during, and after the surgery as it has been shown to improve patient anxiety and overall satisfaction.

NCT ID: NCT02395094 Completed - Clinical trials for Preoperative, Anxiety

Study to Examine the Effects of Child Life Interventions on Children's Anxiety Levels at Induction of Anesthesia

ChildLife
Start date: April 2015
Phase: N/A
Study type: Interventional

Children can experience high levels of anxiety immediately prior to surgery. In fact, this can be the most stressful part of the whole surgical experience for children. Anxiety before surgery is associated with problems after surgery; such as short-term increased need for pain medication and long-term sleep disturbances or behaviour change. Child Life, a program run in some North American children's hospitals has developed ways to reduce children's anxiety prior to surgery. These techniques can include role-play or story books amongst others. In this study, the investigators aim to look at the benefits of the Child Life techniques on anxiety levels of children and their caregivers just prior to receiving anesthesia in the operating room. The study will include children between the ages of 3 and 10 years old, needing day case surgery lasting less than 2 hours, and having never had surgery before. They will be randomly allocated to either not receive any intervention by Child Life or to receive Child Life intervention in the period prior to their surgery, when they are waiting in the Surgical Day Care Unit. Anxiety levels of the children and their caregivers will be measured as they arrive in the hospital and immediately prior to anesthesia, to see if there is a lower level of anxiety in the group receiving the Child Life intervention.

NCT ID: NCT01688115 Completed - Clinical trials for Preoperative Anxiety

Reduction of Preoperative Anxiety in Children: Clickamico Project 2nd Phase

Start date: September 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of a video shown using an iPad, compared to a standard treatment, to reduce preoperative anxiety in children who have to undergo to elective surgery procedure

NCT ID: NCT00816699 Completed - Clinical trials for Preoperative Anxiety

Effects of Providing Preprint Preoperative Anesthetic Risk Information

Start date: December 2008
Phase: Phase 1/Phase 2
Study type: Interventional

Proportion of patients in study group(preprint preoperative anesthetic risk should have more anxiety, more knowledge, and more cancellation than controlled group