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NCT ID: NCT04707521 Completed - Clinical trials for The Fixation Mainly Plays a Firm Role in the Tracheal Intubation and Reduces the Occurrence of Complications

Application of Ship - Shaped Adhesive Tape Fixing in Patients Undergoing Tracheal Intubation

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

In order to evaluate the safety and value of the improved ship-shaped fixing on tracheal intubation patients and provide theoretical basis for clinical therapy, we conducted this research to compare the fixed effectiveness, complications, nursing workload and medical expenses about application of ship-shaped adhesive tape fixation on patient undergoing tracheal intubation.

NCT ID: NCT04707430 Completed - Clinical trials for Relationship of Progesterone Levels and Pregnancy

The Effect of Progesterone Levels on Pregnancy

Start date: August 1, 2020
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to investigate the effect of progesterone levels on pregnancy occurrence on the 3rd and 5th days after insemination.

NCT ID: NCT04707417 Completed - Quality of Life Clinical Trials

Home Care in Allogeneic Haematopoietic Stem Cell Transplantation

Start date: February 1, 2022
Phase:
Study type: Observational

Mixed methods study with focus groups interviews and a prospective observational cohort study aimed to investigate the impact of advanced home care on transplant specific outcomes and quality of life in recipients of allogeneic hematopoietic stem cell transplantation

NCT ID: NCT04707274 Completed - Gluteal Tendinitis Clinical Trials

Reliability, Validity, and Cross-cultural Adaptation of the Turkish Version of the Victorian Institute of Sports Assessment for Gluteal Tendinopathy (VISA-G) Questionnaire

Start date: February 10, 2021
Phase:
Study type: Observational

The purpose of this study was to investigate adaptation, validity, and reliability of the Turkish version of the Victorian Institute of Sports Assessment for Gluteal Tendinopathy (VISA-G) Questionnaire.

NCT ID: NCT04707040 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Neurocognitive Exercise Program for Children With Attention Deficit and Hyperactivity Disorder

Start date: January 8, 2018
Phase: N/A
Study type: Interventional

The effects of Neurocognitive Exercise Program (NEP) on ADHD symptoms and executive functions in children with Attention Deficit and Hyperactivity Disorder (ADHD) will be investigated using The Conners parent rating scale-revised short (CPRS-RS), Stroop Test, Wisconsin test and Y-Balance test.

NCT ID: NCT04706884 Completed - Clinical trials for Etiology of Hyperlactathemia

NEW MONITORING IN DIFFERENTIAL DIAGNOSIS OF HYPERLACTATHEMIA IN CARDIOPULMONARY BYPASS SURGERY

Start date: March 1, 2018
Phase:
Study type: Observational [Patient Registry]

Objective: The objective of the study was to investigate a reverse correlation between blood lactate levels and rSO2, and distinguish between hypoxic and non-hypoxic hyperlactatemia seen in the early postoperative period.

NCT ID: NCT04706767 Completed - Dexmedetomidine Clinical Trials

Effect of Co-administration Lidocaine and Dexmedetomidine on Quality of Recovery

Start date: January 28, 2021
Phase: N/A
Study type: Interventional

BACKGROUND: Some studies have revealed that intravenous (IV) lidocaine or dexmedetomidine might improve the quality of recovery undergoing laparoscopic surgery. The investigators investigated whether co-administration lidocaine and dexmedetomidine could better improve the the quality of recovery after laparoscopic total hysterectomy. METHODS: One hundred and forty-four women with elective laparoscopic total hysterectomy were randomly divided into four groups: Patients in group L received a bolus infusion of lidocaine (2%; 1.5 mg/kg over 10 min before the induction of anesthesia), and then lidocaine was infused at a rate of 1.5 mg/kg/h until close the pneumoperitoneum. Patients in group D received a bolus infusion of dexmedetomidine (0.5 µg/kg over 10 min before the induction of anesthesia), and then dexmedetomidine was infused at a rate of 0.4 μg/kg/h until close the pneumoperitoneum. Patients in group LD received a bolus infusion of lidocaine (2%; 1.5 mg/kg) and dexmedetomidine (0.5 µg/kg) over 10 min before the induction of anesthesia, and then lidocaine and dexmedetomidine were infused at a rate of 1.5 mg/kg/h and 0.4 µg/kg/h until close the pneumoperitoneum, respectively. Patients in group C received the same volume of normal saline 10 min before the induction of anesthesia, and then normal saline (0.9%) was continuously infused in an equal volume until close the pneumoperitoneum. Primary outcome was the quality of recovery (QoR-40) at 1 day prior to sugery, 1 day after sugery, and 2 days after sugery. The secondary outcomes included perioperative remifentanil consumption, postoperative VAS scores, the incidence of postoperative nausea and vomiting, postoperative rescue analgesics and anti-emetics, recovery time, extubation time, and Ramsay sedation scale at 5 min, 10min, 30 min, 60 min after extubation.

NCT ID: NCT04705883 Completed - Breast Cancer Clinical Trials

Vaginal Prasterone In Vaginal Atrophy In Breast Cancer Survivors

VIBRA
Start date: September 1, 2020
Phase: Phase 4
Study type: Interventional

VAGINAL PRASTERONE in the treatment of VAGINAL ATROPHY IN PATIENTS WITH BREAST CANCER TREATMENT WITH AROMATASE INHIBITORS (VIBRA STUDY)

NCT ID: NCT04705675 Completed - Breastfeeding Clinical Trials

The Impact of Breastfeeding Education on Breastfeeding Behavior and the Use of Traditional Practices

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

H1a: The breastfeeding education has an effect the behaviors of mothers toward breastfeeding. H1b: The breastfeeding education has an effect on the use of traditional breastfeeding practices. H0a: The breastfeeding education has not an effect the behaviors of mothers toward breastfeeding. H0b: The breastfeeding education has not an effect on the use of traditional breastfeeding practices.

NCT ID: NCT04705610 Completed - Healthy Clinical Trials

Social Cognition in Multiple Sclerosis, From a Study of Eye Movement and Gaze Strategies Using Video-oculography

EYE-SEP
Start date: May 23, 2017
Phase: N/A
Study type: Interventional

This study aims to: - analyze prospectively the prevalence of subclinical oculomotor disorders (OMDs) in different phenotypes of Multiple Sclerosis (MS) and to study correlations with brain MRI T2 data. - highlight link between modification of visual exploration strategies to decode emotions, and social behavioral disorders, in patients with demyelinating disease, from early to clinically definite stages.