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NCT ID: NCT04467307 Recruiting - Clinical trials for Foreign Body Aspiration, Blood Gas, Bronchoscopy

Comparison of Patients With and Without Foreign Body Aspiration After Bronchoscopy.

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

To compare patients under 5 years of age with foreign body aspiration and without foreign body aspiration with radiological and blood gas results.

NCT ID: NCT04466995 Completed - Clinical trials for Intubation Complication

Factors Affecting Endotracheal Cuff Pressure in Gynecological Cases

Start date: February 5, 2020
Phase: N/A
Study type: Interventional

Postoperative airway complications associated with endotracheal intubation can be seen. While some of these complications are predictable, some may occur urgently. If the endotracheal cuff is over-inflated and its pressure is high, mucosal damage resulting from mucosal pressure is one of the main factors for tracheal morbidity. Endotracheal tube cuff pressure is not routinely measured. It was confirmed that the palpation of the pilot balloon was insufficient to detect high cuff pressures. In laparoscopic cases, the investigators aimed to investigate whether the increase in intra-abdominal pressure as a result of carbon dioxide insufflation, and the change of respiratory functions after trendelenburg position are effective on cuff pressure and whether there is a difference compared to laparotomic cases.

NCT ID: NCT04466319 Completed - Postoperative Ileus Clinical Trials

The Effect of Rocking Chair Movement on the Start of Bowel Functions in Patients With Gastrointestinal System Surgery

Start date: March 15, 2019
Phase: N/A
Study type: Interventional

The Effect of Rocking Chair Movement on the Start of Bowel Functions in Patients With Gastrointestinal System Surgery The research will be carried out as a randomized controlled experimental study in patients with open gastrointestinal tract surgery in order to evaluate the effect of rocking chair movement to be given in addition to standard care in the initiation of postoperative bowel functions (post-operative first time gas, first time defecation).Ethics committee and institution permissions and written consents of individuals were obtained prior to the study.The universe of the study was composed of patients with open gastrointestinal surgery lying in the general surgery service of a hospital in Eskisehir. With the error margin of 0.05, 90% test power, 30 people in intervention and control groups, 60 patients in total will be included in the research.Appointment of patients to intervention and control groups was done by stratification and block randomization method according to gastric and intestinal surgery.The draw method was used to assign stratified patients to blind technique intervention and control groups in order to avoid side-holding, and an equal number (blocking) patients were assigned to each group. The individuals in the intervention group in the rocking chair three times a day, 20 minutes, a total of 60 minutes after the first day after surgery. The individuals in the control group will sit in a standard chair in the same time as the intervention group in the non-rocking chair. The data will be collected using the "Descriptive characteristics determination form", "Intervention Group Intestinal Functions Evaluation Form" and "Control Group Intestinal Functions Evaluation Form".

NCT ID: NCT04466202 Completed - Pain Clinical Trials

Effectiveness of the Music With Structured Verbal Training During Prostate Biopsy

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

Transrectal ultrasound (TRUS) guided prostate biopsy is a gold standard method widely used in the diagnosis of prostate cancer. This procedure can be very painful and anxious for men. Various pharmacological methods can be used to relieve patients' pain and discomfort during TRUS-guided prostate biopsy. Although there is still no consensus on the solution suggestions for pain and anxiety due to biopsy, it is known that music, which is a non-pharmacological method, is effective in this regard. The aim of this study is to evaluate the effect of music with structured verbal training on patients' pain, anxiety and satisfaction levels during transrectal ultrasound-guided prostate biopsy.

NCT ID: NCT04465903 Completed - Swallowing Disorder Clinical Trials

Validity and Reliability of the Turkish Version of the Sydney Swallow Questionnaire

Start date: July 30, 2020
Phase:
Study type: Observational

Purpose of the study is the validity and reliability of the Turkish version of the Sydney Swallow Questionnaire (SSQ-T), so that it would be used as an assessment tool for Turkish dysphagia patients. Despite being translated and validated in many languages, there is no validated Turkish version of SSQ to measure the severity of oropharyngeal dysphagia.

NCT ID: NCT04465006 Completed - Stroke Clinical Trials

Efficacy of Hippotherapy Simulator Exercise Program in Stroke Patients

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

The aim of our study is to investigate the effects of hippotherapy simulator exercises in addition to the conventional rehabilitation program on the balance, postural control, mobility, functional capacity, and independence levels of stroke patients.

NCT ID: NCT04464226 Recruiting - Cancer Clinical Trials

Study to Continue Treatment With Darolutamide in Patients Who Have Been Participating in Previous Darolutamide Studies Supported by Bayer

Start date: October 20, 2020
Phase: Phase 3
Study type: Interventional

The aim of this study is to provide darolutamide treatment to patients who participated in a previous study with darolutamide supported by Bayer and the treating doctor considers that the continuation of the treatment with darolutamide to be beneficial. Patients will be carried over from the previous studies and continue in this study with darolutamide treatment on the same dosage. They will also return to the study centers for doctor's visits as often as they did in the previous study.

NCT ID: NCT04464018 Completed - Clinical trials for Educational Problems

Nurse,Intramuscular Injection, Hybrid Simulation

Start date: January 17, 2018
Phase: N/A
Study type: Interventional

The study was conducted as a randomized controlled experimental study in order to determine the effect of hybrid simulation training on gaining the intramuscular injection skills of nursing students. The sample of the study consisted of 126 students (63 study groups, 63 control groups) enrolled in Nursing Principles Course at Pamukkale University Faculty of Health Sciences in 2018-2019 academic year. In the study, the study group performed hybrid simulation (standard patient+Digital half hip model simulator) and the control group performed simulation with low reality simulation method (hip/intramuscular model). Study data were collected using Student Identification Form, Intramuscular Injection Achievement Test, Intramuscular Injection Application Skill Assessment Form, Two Column Writing Reflective Thinking Strategies and Scale of Student Satisfaction and Self-confidence in Learning.

NCT ID: NCT04463927 Completed - Pain Clinical Trials

The Effect of Non-nutritive Sucking on Pain During Examination for Retinopathy of Prematurity

Start date: May 10, 2020
Phase: N/A
Study type: Interventional

Aim: The aim of the study is to determine the effect of non-nutritive sucking on pain during examination for retinopathy of prematurity. Method: The study is conducted as a randomized controlled trial. The population of the study is premature newborn who treatment in a neonatal intensive unit. The premature newborns divided into two groups as an intervention and control group according to randomization. After the randomization, non-nutritive sucking is applied to the intervention group. No method is applied to the control group.

NCT ID: NCT04463485 Completed - Healthy Clinical Trials

Impact of Umbilical Cord Clamping Time on Infant Anemia

Start date: December 21, 2017
Phase: N/A
Study type: Interventional

This research was conducted to carry out the effect of umbilical cord clamping time on baby anemia.