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NCT ID: NCT05432570 Completed - Clinical trials for Intubation; Difficult or Failed

Use of Muscle Relaxants in Parotidectomy Operation With Neuromonitoring

Start date: June 30, 2022
Phase: N/A
Study type: Interventional

Neuromuscular blockers provide muscle relaxation by blocking the electrical conduction to motor nerves and facilitate endotracheal tube placement while relaxing the whole body for surgical comfort during general anesthesia. Parotid surgery is a procedure performed by ear, nose and throat physicians, and as a complication during this procedure, permanent facial paralysis may develop due to damage to the facial nerve. Intraoperative nerve monitoring is frequently used to avoid this complication. The application of local anesthetic to the vocal cords and into the trachea has been tried and found useful for induction of anesthesia without the use of neuromuscular blockers. In studies conducted with this technique, a standard local anesthetic dose was not specified and local anesthetics were generally administered alone and in high doses. It is expected that anesthesia induction and intubation without the use of muscle relaxants will not affect the comfort of the patient and the procedure, but will increase the surgical time and surgical satisfaction.

NCT ID: NCT05430321 Completed - Preterm Labor Clinical Trials

The Effect of Facilitated Tucking After Vaginal Delivery on Late Preterm Stress, Comfort and Physiological Parameters

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Objective: It is aimed to examine the effect of facilitated tucking after vaginal delivery on late preterm stress, comfort and physiological parameters. Design: The study was designed randomized controlled study. Setting: The study was conducted spontaneous vaginal delivery of late preterm at State Hospital between January-June 2020. Participants: In order to determine the sample size of the study, power analysis was performed using the G*Power (v3.1, 7) program, and a total of 60 preterm were sampled, facilitated tucking (n=30) and control group (n=30). Methods: In the study, Newborn Information and Registration Form, Neonatal Comfort Behavior Scale (NCBS) and Newborn Stress Scale (NSS) were used. As for physiological parameters, for the temperature is used private digital thermometer, for the saturation and heart rate is used device preferred in hospital routine and lastly the respirator rate is clocked by nurses.

NCT ID: NCT05428085 Completed - Clinical trials for Attention-Deficit-Disordered Children

Digital Media Usage With Impulsivity and Attention Deficit in Children

Start date: June 22, 2022
Phase:
Study type: Observational

To explore the relationship between children's digital media usage and attention, activity, parenting pressure; to explore the relationship between family basic data factors and screen usage.

NCT ID: NCT05427773 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

(In)Voluntary Assessed Quadriceps Muscle Endurance in COPD

Bionic
Start date: July 5, 2022
Phase:
Study type: Observational

The primary objective is to assess the relation between involuntary and voluntary assessed quadriceps muscle endurance in patients with COPD. We hypothesized a good correlation (>0.8) between the measurements.

NCT ID: NCT05427149 Completed - Clinical trials for Cesarean Section Complications

The Effect of Intrathecal Magnesium Sulfate on Shivering

Start date: May 10, 2022
Phase: N/A
Study type: Interventional

Shivering after spinal anesthesia is a common complication. Mangesium sulfate, which can be used intrathecally, is effective in preventing tremor. But what is the ideal dose?

NCT ID: NCT05426564 Completed - Thrombosis Clinical Trials

Exploratory Assessment of the Quantra® System in Adult ECMO Patients

Start date: September 27, 2022
Phase:
Study type: Observational

This is a prospective, observational exploratory study of the performance of the Quantra System in adult patients that are undergoing an arterio-venous (AV), veno-venous (VV) ECMO or extra-corporeal life support (ECLS) procedure.

NCT ID: NCT05426382 Completed - Clinical trials for Non Alcoholic Fatty Liver Disease

A Digital Solution for Individuals With Non Alcoholic Fatty Liver Disease

Start date: June 20, 2022
Phase: N/A
Study type: Interventional

Sidekick Health has developed a digital behavioral change program (SK-241) specifically designed for people with metabolic derangements and non-alcoholic fatty liver disease (NAFLD). The SK-241 is delivered through a mobile application and aims at improving lifestyle and health outcomes by focusing on improving diet, increasing activity levels and reducing stress. In this study, the feasibility of the newly developed digital behavioral change program (SK-241) will be evaluated in a minimum of 30 individuals with a NAFLD diagnosis. The primary aim is to explore the acceptability of the SK-241 program by its users, in addition to exploring changes in clinical outcomes and medication adherence after a 12-week intervention with 6 months follow up.

NCT ID: NCT05426148 Completed - Cervical Cancer Clinical Trials

Lot Consistency Clinical Trial of of Recombinant HPV Bivalent Vaccine in 9 to14 Years Old Healthy Female

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

This study is to evaluate lot-lot consistency of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) .

NCT ID: NCT05425199 Completed - Clinical trials for Benign Paroxysmal Positional Vertigo

Habituation Exercises Versus Proprioceptive Training in Benign Paroxysmal Positional Vertigo

Start date: June 5, 2022
Phase: N/A
Study type: Interventional

The aim of this research is to compare the effects of habituation exercises versus proprioceptive training on vertigo, balance, dizziness and quality of life in the individuals having benign paroxysmal positional vertigo. A randomized controlled trial that will include total 39 participants .The first group will receive habituation exercises for six weeks, three times per week for thirty minutes, along with conventional vestibular rehabilitation therapy. The second group will receive proprioceptive training for six weeks, three times per week for 30 minutes, along with vestibular rehabilitation therapy. The third group will only receive vestibular rehabilitation therapy. Data collected will be analyzed through SPSS 25.

NCT ID: NCT05424796 Completed - Clinical trials for Symptomatic Irreversible Pulpitis

Postoperative Pain Intensity After Pulpotomy

Start date: February 15, 2021
Phase: Phase 4
Study type: Interventional

Introduction: This study aimed to compare postoperative pain rates following sodium hypochlorite (NaOCl) and KTP laser-assisted pulpotomy treatments in permanent teeth with deep caries, and symptomatic irreversible pulpitis. Methods: Ninety patients complaining of permanent teeth pain due to symptomatic irreversible pulpitis were randomly divided into 3 equal groups. Preoperative pain levels were recorded. After the initial bleeding control was achieved with saline, complete hemostasis was achieved by applying saline (control group), 2.5% NaOCl, or KTP laser according to randomly determined patient groups. Patients were asked to mark their pain level on the visual pain scale at the 6th, 24th, 48th, and 72nd hours, and 7th and 30th days depending on the severity of the pain. The permanent restoration was completed after 7 days. Results: According to the present study, the statistical difference between the groups in terms of preoperative pain and percussion pain levels was insignificant. There was no significant difference between the groups in terms of demographic data. The postoperative pain level of the KTP laser group was significantly lower at the 6th hour compared to the saline group. There was no significant difference between the groups in terms of postoperative pain level at other time intervals. The greatest pain scores occurred in all groups at 6th hour. Conclusions: KTP laser can be preferred primarily in reducing postoperative pain in pulpotomy treatments. KTP laser or NaOCl assisted pulpotomy can be an effective treatment for pain reduction in permanent teeth with symptomatic irreversible pulpitis.