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NCT ID: NCT03475927 Completed - Radiation Hazard Clinical Trials

Knowledge and Awareness of Radiation Hazard in Health-care Personnel

Start date: April 1, 2018
Phase:
Study type: Observational

Knowledge and awareness of radiation hazard in health-care personnel; A Quaternary-care academic center study Aim: To determine knowledge and concerning about radiation hazard in anesthetic personnel and surgeon study decide: questionnaire based study to ask concerning and knowledge about radiation hazard

NCT ID: NCT03477266 Completed - Clinical trials for Prevention of Postoperative Ileus

Mouth Dissolving Mosapride Tables Enhance Post Cesarean Gut Recovery

Start date: April 1, 2018
Phase: Phase 3
Study type: Interventional

Giving women one day before and immediately after cesarean section a mouthly dissolving mosapride tablets 2every every 8 hours for maximum of 5 days ,or getting recovered gastrointestinal functions And assess preoperative gastrointestinal functions

NCT ID: NCT03482947 Completed - Analgesia, Epidural Clinical Trials

TAP vs Caudal Block Using Dexmedetomidine/ Bupivacaine for Post Operative Analgesia

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

Caudal epidural block is a well-established and commonly performed regional neuraxial technique for providing intraoperative and postoperative analgesia in children scheduled for lower abdomen/perineal surgical interventions. Although the efficacy and safety of Caudal epidural block are fairly high, the associated complications, such as inadvertent dural puncture, unwarranted motor blockade of the lower limbs, and disturbance of bladder function, limit its use. Furthermore, a major limitation of an uncomplicated Caudal epidural block when administered as a "single-shot" technique is its brief duration of action (up to 6 hours), which makes administration of additional analgesics necessary .

NCT ID: NCT03483168 Completed - Clinical trials for Chronic Low Back Pain

Culturally Sensitive Pain Education Program for Turkish Patients

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

In last decade, the awareness has grown regarding the pain neuroscience education (PNE). In the literature, it has been found that there is strong evidence that the educational strategy of pain neuroscience education (PNE) can have positive effects on pain, disability, catastrophization, and physical performance in chronic musculoskeletal disorders. Nowadays, many physiotherapists integrate the PNE into the treatment of chronic pain. However, the importance of culturally sensitive approaches for the treatment of chronic pain has been proposed depending on the cultural differences of pain beliefs, pain cognitions, pain experiences and pain coping strategies in different ethnic populations. Therefore, the aim of this study is to compare the effects of a culturally sensitive PNE with a standard translated PNE on pain intensity, disability status, pain pressure thresholds and psychosocial factors (conceptualization of pain, pain beliefs, catastrophizing, kinesiophobia and illness perception) in Turkish patients with chronic low back pain (LBP). The effects of culturally sensitive PNE format will be compared with the standard translated PNE in a pilot trial. 40 Turkish patients (first generation migrant living around Ghent) with chronic LBP, between the age of 18 and 65 years, will be randomized to the culturally sensitive PNE or standard translated PNE. The content of 2 sessions PNE include the explanation about differences of acute and chronic pain, purpose of acute pain, production of acute pain and chronic pain, and potential sustaining factors for central sensitization, but presented in different ways. They will be subjected to an individual education session and they will receive a home education program. In session 2 (after 1 week), they will come back to ascertain that everything is understood.

NCT ID: NCT03483285 Completed - Clinical trials for Intubation;Difficult

Comparison of Two Different Videolaryngoscopes Regarding Hemodynamic Parameters in Open Heart Surgey

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

Endotracheal intubation increased the heart rate and blood pressure in normal patients. Open heart surgery patients are more prone to hemodynamic variability. In addition, they have increased possibility for difficult intubation The heart rate and blood pressure increase impaired the oxygen consumption. This was previously shown that Videolaryngoscopes minimaly effects the vital signs in normal patients. Videolaryngoscopy inreased the rate of success in normal and difficult airway. This study aimed to compare two laryngoscopes regarding hemodynamic parameters and intubation times in coronary bypass surgery.

NCT ID: NCT03484260 Completed - Hypogonadism Clinical Trials

Association Between the Prevalence of Cardiovascular Risk Factors and New Use of Testosterone

Start date: April 1, 2018
Phase:
Study type: Observational

We will investigate if testosterone is preferentially given to patients at higher risk of cardiovascular events. If this is the case, then observational studies may be prone to selection bias resulting in overestimation of the cardiovascular risk associated with testosterone when compared to a healthier population not taking testosterone

NCT ID: NCT03484806 Completed - Clinical trials for Valvular Heart Disease

The China Valvular Heart Disease Study

China-VHD
Start date: April 1, 2018
Phase:
Study type: Observational [Patient Registry]

This is a observational、multicenter, prospective cohort study for adults with significant VHD. The purposes of this study were to evaluate the etiology、clinical characteristics、treatment modalities, and outcomes of patients with VHD;also to set up registration system of adult VHD in China, to build a database of Chinese adult VHD, to establish a web-based international standard data acquisition system for VHD and a multicenter clinical research platform. The results of the study will provide a basis for the future national health policy for prevention and treatment of adult VHD.

NCT ID: NCT03487341 Completed - Blood Loss Clinical Trials

Placental Cord Drainage After Vaginal Delivery

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

Placental Cord Drainage after Vaginal Delivery A randomized clinical trial

NCT ID: NCT03487354 Completed - Miscarriage Clinical Trials

Medical Abortion With Single Daily Dose of Misoprostol

Start date: April 1, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

Medical abortion using multiple vs single daily dose of misoprostol in first trimester miscarriage.

NCT ID: NCT03491384 Completed - Anxiety Clinical Trials

Anxiety, Inflammation, and Stress

Start date: April 1, 2018
Phase:
Study type: Observational

This study investigates whether the anxiolytic effects and anti-inflammatory properties of cannabis vary as a function of the ratio of CBD to THC, with the goal that these effects may shed light on the mixed data linking cannabis use and anxiety. Individuals with mild to moderate anxiety who elect to use cannabis (smoked flower or edible) will complete four weeks of observation. Participants complete cognitive tasks, a substance use history, health questionnaires concerning sleep and physical activity, and a blood draw at four different time points (Baseline, after 2 weeks of cannabis use, and immediately before and after self-administration after 4 weeks of use) with the use of a mobile pharmacology laboratory, which goes to a convenient location for each participant to self-administer their cannabis. Participants are then followed for five months to self-report on cannabis use, anxiety, subjective cognitive functioning, sleep quality, and other mental health symptoms.