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NCT ID: NCT04445675 Not yet recruiting - Jaundice, Neonatal Clinical Trials

The Effect of Breastfeeding Support on Hospitalization Due to Jaundice

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

Neonatal jaundice is the most common reason for rehospitalization after postnatal discharge. Jaundice due to breastfeeding failure is an important subtype of pathological neonatal jaundice. Typically, it occurs with lactation failure, which results in dehydration (reducing urine output), significant weight loss (>10% of birth weight) and sometimes hypernatremia, during the first postnatal week. Jaundice caused by breastfeeding failure is observed in one third (31.8%) of total cases of pathological neonatal jaundice requiring rehospitalization. Jaundice lasts for an average of 6.8 days and the length of hospital stay takes up to 3 days. Jaundice due to breastfeeding failure requires focused efforts for a program structured with breastfeeding education and special breastfeeding support. This support causes the role of nurses to become even more important. The aim of this study is to investigate the effect of support provided for breastfeeding and the feeding of infants' with breast milk on hospitalization due to jaundice. Research Hypotheses: H0: The support provided for breastfeeding and the feeding of infants' with breast milk has no effect on hospitalization due to jaundice. H1: The support provided for breastfeeding and the feeding of infants' with breast milk affects the consequences of hospitalization due to jaundice.

NCT ID: NCT04444986 Completed - Bioequivalence Clinical Trials

Bioequivalence Study of Favir 200 mg Film Tablet Kocak Under Fasting Conditions

Start date: June 5, 2020
Phase: Phase 1
Study type: Interventional

A single dose of Reference product containing 200 mg favipiravir and a single dose of Test product containing 200 mg favipiravir or vice versa; administered with 240 mL of water at room temperature, in each period under fasting conditions with current pandemic precautions.

NCT ID: NCT04444557 Completed - Depression Clinical Trials

Effect of COvid-19 on Mental Health in Syrian and Turkish Maintenance HemoDialysis Patients: COST-HD Study

COST-HD
Start date: April 17, 2020
Phase:
Study type: Observational

SARS-COV infection first has begun at Wuhan, China, and then became a pandemic. The first COVID-19 case has been reported on March 11, 2020, in Turkey. People older than 65 years old have been locked down on March 21 and people younger than 20 years old locked down at April 03. A total lockdown has been done a few times lasting for 3 or 4 days, especially at weekends. Renal replacement modalities have been affected in different ways during the pandemic. Patients with kidney transplantation and patients performing home hemodialysis or peritoneal dialysis have been advised to perform self-isolation at homes. However, center hemodialysis patients continued to come dialysis centers obligatorily. Syrian civil war has been continuing since 2011, and Turkey has accepted millions of Syrian people in a position called temporary protection. There are many Syrian center hemodialysis patients both in Turkey and in our unit. The investigators do not know if pandemic affected Syrian patients different than Turkish ones. The aim of this study is to compare beck depression scores of Turkish and Syrian patients undergoing hemodialysis during the COVID-19 pandemic.

NCT ID: NCT04444375 Completed - Diabetes Mellitus Clinical Trials

Plantar Pain, Balance and Foot Function in Individuals With Diabetes Mellitus

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

Diabetes Mellitus (DM) and increase of body mass index (BMI) are two one of the most common risk factors for plantar pain and related disability. The aim of our study was to evaluate the relationship between plantar pain, balance and foot function in diabetic DM patients has with different BMI.

NCT ID: NCT04444258 Completed - Clinical trials for Educational Problems

Teaching Fetal Development With Virtual Reality

Start date: March 15, 2020
Phase: N/A
Study type: Interventional

In this study, it was aimed to design virtual pregnancy for pregnancy formation, fetal and placental development in the virtual reality environment and to evaluate the effectiveness of the designed virtual pregnancy on midwifery education. Our study, which will be the first in our second country in the world, aims to reduce the application errors and determine deviations from normal by examining the formation of pregnancy, maternal, fetal and placental changes, which form the basis of midwifery profession, before having clinical experience. In this direction, the objectives of our study are; - Development of the virtual pregnancy application, which will be designed for the first time in our country, - Ensuring the effective use of virtual pregnancy practice in midwifery education, - Visualizing fetal and placental development with virtual pregnancy that will form the basis of midwifery education, - To minimize the application errors experienced in clinical practices of midwifery students, - To increase educational effectiveness, clinical and academic success by visualizing the formation of pregnancy. - Measuring cognitive loadings of students after education - Measuring students' sense of readiness

NCT ID: NCT04443556 Completed - Postoperative Pain Clinical Trials

Effect of Continue RISS Block in Thoracotomy

Start date: August 31, 2020
Phase: N/A
Study type: Interventional

Thoracotomy is one of the most painful surgery. Acute postoperative pain increases postoperative morbidity and prolongs hospital stay and also may lead to developing a chronic pain syndrome. This study aimed to assess the efficacy of continuous rhomboid intercostal and subserratus plane (RISS) block by inserting a catheter under direct vision for controlling acute thoracotomy pain.

NCT ID: NCT04443374 Completed - Clinical trials for Psychiatric Disorder

The Turkish Version of the Simple Physical Activity Questionnaire (SIMPAQ)

SIMPAQ
Start date: June 30, 2020
Phase:
Study type: Observational

The Simple Physical Activity Questionnaire (SIMPAQ) was originally developed in English to assess physical activity level particularly people with mental illnesses. The purpose of this study was to translate and cross-culturally adapt the SIMPAQ into Turkish and investigate its psychometric properties.

NCT ID: NCT04443140 Completed - Covid-19 Clinical Trials

Preeclampsia-like Syndrome Induced by COVID-19: Is it a Real Public Health Issue in Pregnancy During the Pandemic?

Start date: March 15, 2020
Phase:
Study type: Observational [Patient Registry]

By applying polymerase chain reaction (PCR) test for Covid-19 to preeclampsia patients who applied to our hospital during the Covid-19 pandemic period, we investigated the frequency of Covid-19 related preeclampsia-like syndrome in this patient group.

NCT ID: NCT04442958 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Effectiveness of Convalescent Immune Plasma Therapy

Start date: May 15, 2020
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the safety, improvement of clinical symptoms and laboratory parameters of convalescent immune plasma treatment in severe Covid-19 patients with ARDS.

NCT ID: NCT04442009 Withdrawn - Clinical trials for Maxillofacial Abnormalities

Superficial Cervical Plexus Block for Orthognathic Surgery

Start date: June 22, 2020
Phase: N/A
Study type: Interventional

US-guided superficial cervical plexus block (SCPB) may be used for several head and neck surgeries. Local anesthetic is injected under the sternocleidomastoid muscle for SCPB. It has lower complication rate compared to the deep cervical plexus block. Postoperative pain management is important in patients underwent orthognathic surgery. Effective pain treatment provides early mobilization, and shorter hospital stay.