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NCT ID: NCT06404879 Not yet recruiting - Anxiety Clinical Trials

The Effect of Parental Anxiety Level on the Child's Anxiety Level and Postoperative Pain in Children Undergoing Surgery.

Start date: May 30, 2024
Phase:
Study type: Observational [Patient Registry]

The aim of this prospective study is to investigate whether the anxiety levels of parents of children aged 2-6 years who will undergo inguinal area surgery have an effect on the child's preoperative anxiety level and postoperative pain level.

NCT ID: NCT06404827 Not yet recruiting - Cerebral Palsy Clinical Trials

The Effect of Hippotherapy Simulator in Children With Spastic Cerebral Palsy

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

The horseback riding simulator (HRS) is a dynamic robotic device that mimics the movement of a horse for hippotherapy purposes. HRS aims to improve the patient's balance, adaptation and provide postural adjustment by mimicking the rhythmic movements of the horse. This study aims to research the potential benefits of the horseback riding simulator on the lower extremity selective motor control, balance and trunk control in children with Cerebral palsy.

NCT ID: NCT06404762 Recruiting - Clinical trials for Gingival Recession, Localized

Tuberosity Versus Palatal Connective Tissue Graft on the Treatment of Single Maxillary Recession-type Defects

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

The goal of this randomized clinical study is to assess the root coverage outcomes and patient morbidity following the treatment of single maxillary recession-type defects using a coronally advanced flap (CAF) combined with a subepithelial connective tissue graft (SCTG) harvested from the maxillary tuberosity (MT) versus lateral palate (LP). The secondary objective is to evaluate the histological characteristics of graft compositions harvested from the different regions (MT versus LP). Therefore, the following questions related to the study are raised: - Do SCTGs harvested from MT (tSCTG) and LP (pSCTG) exhibit similar root coverage outcomes in the treatment of single maxillary recession-type defects using CAF? - What are the histological characteristics of tSCTG and pSCTG? A total of 30 patients who have been referred to the Gazi University Department of Periodontology will be randomly assigned to receive tSCTG or pSCTG in combination with CAF. Clinical measurements will be recorded at baseline, 1, 3, 6, and 12 months after surgeries. Immediately after interventions; a questionnaire evaluating post-operative pain, discomfort, sensitivity, and bleeding will be given to the patients. The amount of non-steroid anti-inflammatory drugs used will be recorded at 1, 2, 3, 7, 14 and 28 days after surgery. Descriptive morphologic analysis of the grafts will be assessed in terms of the presence of inflammatory cells, connective tissue cellularity, vascularization, adipose tissue, and collagen structure.

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.