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NCT ID: NCT06404710 Active, not recruiting - Clinical trials for the Participant Wishes to Leave the Study

Progressive Muscle Relaxation Exercise Applied After Heart Surgery

Start date: October 18, 2023
Phase: N/A
Study type: Interventional

Various methods are used to prolong life and improve quality of life in heart diseases. There are surgical treatment options. Heart surgery is a major surgery and surgery Due to common postoperative symptoms, follow-up and follow-up in the early postoperative period maintenance is important.Progressive relaxation exercise; optimization of analgesia, pain management, reduction of side effects, regulation of vital signs, increase in sleep qualityIt has been reported that it provides positive effects on many systems and increases the success of the surgical process. It has been stated in research that it can increase.In this study, patients who had undergone cardiac surgery and were treated as inpatients progressive muscle relaxation in reducing pain, reducing anxiety, and improving the quality of sleep and recovery It was aimed to determine the effect of the exercises.

NCT ID: NCT06404476 Recruiting - Clinical trials for Periodontal Diseases

Evaluation of Salivary Galectin-8, Galectin-9 and RANKL Levels of Individuals With Different Periodontal Diseases

Start date: May 3, 2024
Phase: N/A
Study type: Interventional

The aim of this study is; detection of Galectin-8, Galectin-9 and RANKL levels in saliva samples of periodontally healthy, gingivitis and periodontitis patients and the possible correlation between these values and clinical parameters of periodontal diseases. Materials and methods: Samples of saliva were obtained from 60 systemically healthy non-smoker individuals with periodontitis (P, n=20), gingivitis(G, n=20) and healthy periodontium (S, n=20). Full-mouth clinical periodontal measurements including probing depth (PD), clinical attachment level (CAL), bleeding on probing (BOP), gingival index (GI) and plaque index (PI) were also recorded. Enzyme-linked immunosorbent assay (ELISA) was used to determine Galectin-8, Galectin-9 and RANKL levels in the biological samples.

NCT ID: NCT06404151 Recruiting - Oxygen Deficiency Clinical Trials

Comparison of Oxygen Reserve Index and Regional Cerebral Oxygen Saturation Indetermining Hypoxia in Obese Patients

Start date: July 1, 2023
Phase:
Study type: Observational

The primary aim of this study is to compare the effectiveness of ORI and rcSO2 in predicting hypoxia early in obese patients who are sensitive to hypoxia. Our secondary aim is; To determine whether there is a correlation between the changing trend of ORI and rcSO2 in obese patients.

NCT ID: NCT06404125 Recruiting - Chronic Pain Clinical Trials

Investigation of the Effect of Central Sensitization Symptom Severity on Steroid Injection Results in Shoulder Pain

Start date: March 1, 2023
Phase:
Study type: Observational

The aim of this study was to investigate the effect of the presence and severity of pre-treatment central sensitization on the results of subacromial/ intra-articular shoulder injection in patients with rotator cuff lesion/subacromial impingement. The hypothesis of the study is that the treatment response will decrease in patients with pre-injection central sensitization. There are many studies investigating the frequency of central sensitization in various shoulder pathologies. However, the effect of this condition, which is likely to be associated with chronic pain in these patients, on treatment response is unknown. The effect on the results of shoulder injection, one of the most common procedures in physical therapy practice, will be investigated.

NCT ID: NCT06403956 Completed - Clinical trials for Complications of Medical and Surgical Care (Y62-Y84)

Students' Hand Hygiene Beliefs, Practices and Skills

SHHBPS
Start date: January 15, 2024
Phase: N/A
Study type: Interventional

ABSTRACT This study was conducted to determine the effect of hand hygiene training given to home patient care students with different methods on their hand hygiene beliefs, practices and skills. This study was a randomized controlled trial. The population of the study consisted of 123 students. After the removals, the study was completed with 75 students in the video, paint and control groups. In the intervention of the study, lecture, discussion, question and answer, demonstration, coloring and video methods were used.

NCT ID: NCT06403891 Recruiting - Cerebral Palsy Clinical Trials

The Effect of a Comprehensive Rehabilitation Program Using Robotic Walking and Functional Electrical Stimulation Technologies on Balance and Walking in Children With Cerebral Palsy

Start date: March 15, 2022
Phase:
Study type: Observational

The aim of this study was to investigate the effect of a comprehensive rehabilitation program using robotic walking and functional electrical stimulation technologies on balance and gait in children with cerebral palsy. This study was planned as a prospective observational study. A total of 30 patients in two groups were planned to be included in the study. Patients in both groups were planned to receive a 6-week conventional rehabilitation program that was prepared to meet the requirements of their clinical conditions, including neurophysiological exercises, balance-coordination and posture exercises. The case group was planned to consist of patients who received a comprehensive rehabilitation program using high-tech devices including functional electrical stimulation (FES) and robotic rehabilitation applications in addition to the conventional rehabilitation program.

NCT ID: NCT06403774 Enrolling by invitation - HEMORRHOIDECTOMY Clinical Trials

Bowel Preparation Before Hemorrhoidectomy

Start date: July 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this research; To evaluate the effect of preoperative bowel preparation on post-hemorrhoidectomy outcomes. Bowel preparation is a routine practice before surgery in anorectal diseases. This study aims to evaluate the effect of bowel preparation using laxatives or enemas on the patient postoperative pain, analgesic consumption amount, comfort, first defecation time and satisfaction, and to evaluate the satisfaction of the surgical team.

NCT ID: NCT06403696 Recruiting - Clinical trials for Airway Complication of Anesthesia

Predicting Post-op Airway Complications in Pediatric Patients Using Ultrasonography

Start date: May 2, 2024
Phase:
Study type: Observational

Laryngospasm and post-extubation stridor are major postoperative airway difficulties in pediatric patients using tracheal tubes. These conditions are frequently caused by epithelium edema and anesthesia-related problems. Because it could reveal tracheal and laryngeal issues, ultrasound is an essential method for establishing the proper endotracheal tube size and minimizing difficulties. This research focuses on the use of ultrasonography to predict and understand pediatric postoperative airway complications.

NCT ID: NCT06403670 Completed - Clinical trials for Comparison of the Effects of Remifentanil and Dexmedetomidine

Dexmedetomidine and Remifentanil in NORA

Start date: December 17, 2022
Phase: Phase 4
Study type: Interventional

Endoscopic retrograde cholangiopancreatography (ERCP) procedure is frequently encountered in non-operating room anesthesia applications (NORA). It is a procedure that requires deep sedation and analgesia in terms of gastroenterologist and patient comfort. Dexmedetomidine, which is increasingly used in NORA applications, comes to the fore because it does not cause respiratory depression, reduces the stress response, and provides hemodynamic stability. This study aims to compare the effects of dexmedetomidine-propofol (DP) and remifentanil-propofol (RP) combinations on hemodynamic stability, rapid recovery, and patient comfort in patients who underwent ERCP.

NCT ID: NCT06403579 Enrolling by invitation - Clinical trials for PAIN, ANXIETY, AND COMFORT

THE EFFECT OF VIRTUAL REALITY APPLICATION ON PAIN, ANXIETY, AND COMFORT DURING CURETTAGE/DILATATION

Start date: May 1, 2024
Phase: N/A
Study type: Interventional

The problems experienced by women at the stage of deciding to have a miscarriage, during and after miscarriage differ and their anxiety levels vary. It was determined that women experienced fear, thinking that they would sin, guilt, regret and indecision at the stage of deciding to abort. methods are used to relieve the pain and anxiety caused by interventional procedures in patients in direct proportion to the development of technology. Virtual reality (VR), one of these methods, is an innovative, up-to-date and unique application, combining reality and imagination with fictional technology.There is no study in the literature on the application of SG during curettage/dilatation procedure. This study was conducted to determine the effect of SG application on pain anxiety and comfort during curettage/dilatation procedure.