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NCT ID: NCT04762563 Completed - Low Back Pain Clinical Trials

Effect of Treatment on Connective Tissue in Low Back Pain

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate the effects of instrument assisted soft tissue mobilization (IASTM) and kinesiology taping (KT) that are additional treatment to the conservative treatment for the lumbar region and hamstrings and connective tissue thickness in patients with chronic non-specific low back pain (CNSLBP).

NCT ID: NCT04762095 Completed - Clinical trials for Postmenopausal Women

The Effect of Mindfulness Stress Reduction Program on Menopausal Complaints and Quality of Life

Start date: March 29, 2019
Phase: N/A
Study type: Interventional

The study was conducted to determine the effect of the mindfulness stress reduction program (MBSR) applied to postmenopausal women on menopausal complaints and quality of life. The population of the study was 2626 women and the sample was composed of 55 experimental and 63 control groups, totally 118 women. The data of the study were collected using Personal Information Form, Mindful Attention Awareness Scale (MAAS), Menopausal Symptoms Assessment Scale (MSAS) and Menopause Specific Quality of Life Scale (MYQOL).

NCT ID: NCT04762056 Completed - Covid19 Clinical Trials

CPAx for Assessing Functional Status of COVID-19 Patients After Intensive Care Unit Discharge

Start date: February 22, 2021
Phase:
Study type: Observational

The present assessment tools for assessing physical function after intensive care unit (ICU) can be categorized as (1) functional tests (2) walk tests (3) strength test (4) Health-related quality of life (HRQOL). Strength tests such as Medical Research Council Scale and HRQOL (e.g. Short form-36 (SF-36) tests may require awakening and appropriate mental health. However, mental impairments were seen in a considerable number of patients (2). Walk tests such as Six-Minute Walk Test (6MWT) or Timed Up&Go (TUG) can be impractical, some patients could not be able to perform these due to severe impairment. These tests require space to perform and may require management of several drips, drains, and oxygen delivery systems while the patient is walking and turning which render the test difficult to carry out. Among these three specific tools, CPAx seems to be the assessment tool that can be considered easy to use in the clinical setting due to the short time required for assessment and relatively minimal use of equipment (hand dynamometer for grip strength measurement). This study aims to investigate validation of Chelsea Critical Care Physical Assessment Tool in the assessment of the functional status of COVID patients discharged from ICU and investigate the feasibility of commonly used assessment tools for assessing physical function after ICU in COVID patients discharged from ICU.

NCT ID: NCT04761159 Completed - Clinical trials for Postoperative Recovery

Ketamin Plus Propofol for Anesthesia Induction

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

ASA I-II 112 pediatric patients will recruit who underwent adenoidectomy-tonsillectomy surgery. Propofol 1 mg/kg + ketamin1 mg/kg (1/1 ratio) for group I; propofol 1,5 mg/kg + ketamin 0,75 mg/kg (2/1 ratio) for group II; propofol 2 mg/kg +ketamin 0,66 mg/kg (3/1 ratio) for group III; propofol 3 mg/kg will perform for anesthesia induction. General anesthesia will maintenance with sevoflurane 1-2% and O2/N2O mixture. Morphine 0.1mg/kg IV will be apply for postoperative analgesia at 10 min of anesthesia. Extubation time, length of stay in PACU, Watcha score, FLACC score will record. Than all data will statistically analyse.

NCT ID: NCT04761029 Completed - Postoperative Pain Clinical Trials

Rhomboid Intercostal and Subserratus Plane Block

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

Laparoscopic surgery is frequently used today for abdominal region operations. Laparoscopy has become the preferred treatment for cholecystectomy. Patients undergoing laparoscopic cholecystectomy suffer from acute postoperative pain despite the multimodal analgesic regimen. For this type of surgery, many different field blocks have been used for postoperative analgesia.

NCT ID: NCT04760626 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Research Study to Compare a New Weekly Insulin, Insulin Icodec Used With DoseGuide App, and Daily Insulins in People With Type 2 Diabetes Who Have Not Used Insulin Before

ONWARDS 5
Start date: March 1, 2021
Phase: Phase 3
Study type: Interventional

This study compares insulin icodec to different daily insulins in people with type 2 diabetes. The study will look at how well insulin icodec taken once weekly controls blood sugar compared to the insulins taken once daily. Participants will either get insulin icodec, that participants will have to inject once a week on the same day of the week, or a marketed insulin, that participants will have to inject once a day. Which treatment participants get is decided at random. The insulin is injected with a needle in a skin fold in the thigh, upper arm or stomach. Participants will measure their blood sugar every day. Participants will get a study phone to record safety data in the electronic diary (eDiary). If participants get a daily insulin they will record their insulin doses in the eDiary. If Participants get weekly insulin icodec, participants study phone will also have the DoseGuide App. The DoseGuide App gives dose recommendations based on their blood sugar and previous doses. Participants will record their insulin doses in the DoseGuide App. The study will last for about 1 year and 2 months. Participants will have 8 planned clinic visits with the study doctor. More visits will be planned to meet individual needs. At 6 clinic visits participants will have blood samples taken. Women cannot take part if pregnant, breast-feeding or plan to become pregnant during the study period.

NCT ID: NCT04760509 Active, not recruiting - Newborn Morbidity Clinical Trials

Short- Term Follow up Of Neonates Born With Neural Tube Defect

STFUONBWNTD
Start date: February 1, 2021
Phase:
Study type: Observational

Neural tube defects (NTD), which is the most common anomaly of the central nervous system, which can be diagnosed during antenatal period, brings many problems both in the neonatal period and in advanced ages. Open neural tube defects, in particular, progress with sensory-motor deficits due to the risk of infection and neural tissue loss from birth, and should be followed closely from the neonatal period. Newborns born with a neural tube defect should be operated within the first 72 hours postnatal and the defect should be closed. In this hospital, newborns with NTD are monitored in our neonatal surgery intensive care unit before and after surgery. Neonatal specialists, neurosurgeons and other specialists when there is an additional anomaly evaluate the baby as multidisciplinary. In this project, the short-term follow-up data of babies with NTD who have been followed up in this neonatal surgery intensive care unit for the last fifteen years will be evaluated retrospectively.

NCT ID: NCT04760262 Completed - Thoracic Surgery Clinical Trials

The Effect of Anesthesia on Cerebral Oxygenation

Start date: March 1, 2017
Phase:
Study type: Observational

One-lung ventilation (OLV) may cause negative changes in the oxygenation of cerebral tissue which results in postoperative cognitive dysfunction. The aim of this prospective study was to compare the potential effects of TIVA and inhalation general anesthesia techniques on cerebral tissue oxygenation and postoperative cognitive functions in patients receiving one-lung ventilation in thoracic surgery

NCT ID: NCT04760158 Completed - Clinical trials for Patello Femoral Syndrome

Comparison of New Technique Taping and Placebo Taping on Patellofemoral Pain Syndrome: A Randomised Controlled Study

Start date: June 5, 2019
Phase: N/A
Study type: Interventional

We included in this study 42 individuals with patellofemoral pain syndrome. 39 of them were completed six weeks of exercise and other groups. We randomized them into three groups. One group is the star technique which is a new patellar taping technique. Another group is placebo taping and the third group is only the exercise group. Both groups performed exercises three times a week for six weeks. Three groups were assessed with knee and hip muscles strength, shortness, performance tests, pain severity in the activity, night, rest, and knee-buckling, and Kujala Scale before and after 4-week exercises.

NCT ID: NCT04760067 Completed - Athletic Injuries Clinical Trials

Comparison of Sport Injury Anxiety of Athletes Doing Sports on Different Surfaces

Start date: February 17, 2021
Phase:
Study type: Observational

Due to its nature, sports are an activity in which injuries are common. Sports injuries have athletic and environmental reasons. In sports injuries, although the medical team is generally interested in the physiological aspect of the injury, in recent years, the psychological aspect of the injury has also started to be taken care of. One of these psychological aspects is anxiety. Athletes who develop sports injury anxiety are more prone to injury. One of the environmental reasons is the ground for sports. We could not find a study in the literature comparing the anxiety levels of those who do sports on different grounds in different sports branches. Our study will provide support to the literature in this direction.