Clinical Trials Logo

Filter by:
NCT ID: NCT06187753 Recruiting - Clinical trials for Eosinophilic Esophagitis

Sensory Processing Issues in Eosinophilic Esophagitis

Start date: August 20, 2023
Phase:
Study type: Observational

Feeding dysfunction and/or dysphagia are the main symptoms of eosinophilic esophagitis (EoE). Also, these symptoms may be a part of sensory processing disorders. Therefore, the present study compared sensory processing abilities between children with EoE and typically developing (TD) controls.

NCT ID: NCT06187714 Recruiting - Clinical trials for Optic Nerve Sheath Diameter

Effect of Caudal Block Injection Rate on Optic Nerve Sheath Diameter in Pediatric Surgeries

Start date: July 5, 2023
Phase:
Study type: Observational

Our prospective observational study will include patients between the ages of 1-7 years, ASA 1-2, who will undergo elective surgery under general anesthesia, whose consent was obtained by their parents for the procedure to be performed. Optic nerve sheath diameter of the patients will be measured and recorded.

NCT ID: NCT06187623 Recruiting - Clinical trials for Adolescent Idiopathic Scoliosis

COMPARISON OF THE EFFECTIVENESS OF CLINICAL AND HOME-BASED SCHROTH EXERCISES ON ADOLESCENT IDIOPATHIC SCOLIOSIS INDIVIDUALS

Start date: December 15, 2023
Phase:
Study type: Observational [Patient Registry]

In individuals diagnosed with AIS, significant regressions in curvature were observed with the use of schroth exercises and brace. It is known that neurological changes affect the vestibular system and create changes in the individual's balance and proprioception. At the same time, when static and balance are examined, it is seen that they have difficulty in maintaining their dynamic balance and their body center of gravity oscillations increase. There are a limited number of studies in the literature evaluating individuals diagnosed with AIS in the combined treatment of brace use and Schroth exercises.

NCT ID: NCT06186908 Recruiting - Clinical trials for Periodontal Diseases

Evaluation of Salivary Gal-7, Gal-10 and MMP-9 Levels of Individuals With Different Periodontal Diseases

Start date: May 2, 2024
Phase: N/A
Study type: Interventional

The aim of this study is; detection of Galectin-10, Galectin-7, MMP-9 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-10, Galectin-7 and MMP-9 levels in the biological samples.

NCT ID: NCT06186830 Recruiting - Clinical trials for Temporomandibular Disorder

Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire (BETY-BQ) in Patient With Temporomandibular Disorders

Start date: December 17, 2023
Phase:
Study type: Observational

The aim of this study is to investigate the validity, reliability, and responsiveness of the Cognitive Exercise Therapy Approach-Biopsychosocial Questionnaire (BETY-BQ) in individuals with temporomandibular disorder. The following are alternative hypotheses of the study: - BETY-BQ has significant convergence with the Patient Health Questionnaire-9 measuring depression. - BETY-BQ has significant convergence with the Patient Health Questionnaire-15 measuring physical symptoms. - BETY-BQ has significant convergence with the Generalized Anxiety Disorder-7 measuring anxiety. - BETY-BQ has significant convergence with the Short Form-36 measuring quality of life. - BETY-BQ has significant convergence with the Craniomandibular Pain and Disability Inventory measuring disability. - BETY-BQ has significant convergence with the Mandibular Function Impairment Questionnaire measuring function. - BETY-BQ has significant stability. - BETY-BQ has significant internal consistency.

NCT ID: NCT06186817 Recruiting - Clinical trials for Temporomandibular Disorder

Effectiveness of the Fascial Distortion Model on the Cervical Spine in Individuals With Temporomandibular Disorder

Start date: December 17, 2023
Phase: N/A
Study type: Interventional

The goal of this randomized clinical trial is to investigate the effectiveness of Manual Therapy Based on the Fascial Distortion Model (FDM) on the cervical spine by comparing it with Core Stabilization Training (CST) or Control in individuals with temporomandibular disorders. The main questions it aims to answer are: Is the effectiveness of the addition of FDM-based Manual Therapy to conventional therapy different from the addition of CST or control? Is the effectiveness of the addition of CST to conventional therapy different from the addition of FDM or control? All participants in the intervention groups will be given eight-week conventional therapy (Rocabado Exercises and Patient Education) in addition to FDM-based Manual Therapy or CST. Participants in the control group will not be given any therapy during the study. Neck pain intensity, hand grip strength, head posture, cervical muscle performance, cervical range of motion (function), disability, and quality of life will be assessed.

NCT ID: NCT06186518 Recruiting - Pain Clinical Trials

The Effect of the PİKSEÇ App on Peripheral Intravenous Catheter Insertion on Success, Pain and Emotional Level in Children

Start date: December 15, 2023
Phase: N/A
Study type: Interventional

The study employed a post-test non-randomized controlled trial to assess the impact of the PİKSEÇ (Peripheral Intravenous Catheter Selection) application on the success of peripheral intravenous catheter (PIVC) placement, as well as on the pain and emotional level scores of hospitalized preschool children aged 3-6 years. In preschool children, aged 3-6 years, who were hospitalized, anxiety about losing body integrity is commonly observed. Children tend to think that all the material inside their bodies can come out through a wound or hole during invasive procedures. Therefore, it becomes crucial to reduce anxiety related to invasive procedures in children of this age group. In this context, the study aimed to be conducted in preschool children.

NCT ID: NCT06186453 Recruiting - Preterm Clinical Trials

Effectiveness of Bonding-Based Education Intervention

Start date: December 15, 2023
Phase: N/A
Study type: Interventional

The study aimed to determine the impact of the Father-Preterm Newborn Bonding Programme (B-PreBAP) on fathers' parenting behaviours, stress levels, and support needs. Additionally, the study aimed to investigate the effect of B-PreBAP on the stress levels of preterm newborns.

NCT ID: NCT06185725 Recruiting - Cesarean Section Clinical Trials

Comparison of Modified Perichondral Approach Thoracoabdominal Nerve Block and Transversus Abdominal Plane Block in Analgesia Management Following Caesarean Section Surgery

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

Cesarean section (CS) is one of the most frequently performed surgical procedures in the World. Moderate to severe postoperative pain occurs in a significant proportion of women after cesarean surgery. The analgesic effectiveness of TAP block has been demonstrated after cesarean section operations. m-TAPA block has been described as an alternative analgesic technique in abdominal surgeries. The aim of this study is to compare these two analgesic methods in terms of effectiveness for postoperative analgesia management after cesarean section.

NCT ID: NCT06185231 Recruiting - Clinical trials for Anterior Cruciate Ligament Injuries

Investigation of the Effects of Vibration Therapy on Pain, Functionality, and Proprioception After ACL Injury

Start date: September 15, 2023
Phase: N/A
Study type: Interventional

Over the past decade, vibration therapy has gained popularity. This treatment involves the transmission of vibration either through whole-body vibration (WBV) platforms or by applying local vibration (LV) directly to the muscles or tendons. In the context of ACLR (anterior cruciate ligament reconstruction), it has been reported that a single session of either WBV or LV, applied while patients maintain a squatting position, acutely improves the strength of the Quadriceps muscle when applied 50 months post-surgery, possibly by reducing arthrogenic muscle inhibition. Another study tested whether local vibration training (LVT) in the early post-ACLR phase (first 10 weeks) could improve strength recovery and found that LVT enhances strength regain after ACLR. This feasibility study demonstrates that LVT applied to relaxed muscles is a promising method of vibration therapy that can be applied early in ACLR. Compared to traditional massage, vibration therapy may also improve strength parameters. Percussion massage therapy is a new method that combines elements of traditional massage and vibration therapy. In the literature, there is a lack of scientific evidence on how and to what extent percussion massage therapy affects range of motion (ROM) and muscle strength. To date, only one conference paper has investigated the effects of a handheld percussion massage therapy device, and they found no change in vertical jump height after a 5-minute percussion massage therapy session applied to several lower body muscle groups." A review of the literature reveals that to date, there has been no study investigating the effects of manually applied percussion massage therapy on pain, functionality, and proprioception in cases who have undergone anterior cruciate ligament surgery. Therefore, the purpose of our study is to examine the effects of percussion massage therapy on pain, joint range of motion, joint position sense, muscle diameter, balance parameters, and functionality in patients who have undergone surgery following an anterior cruciate ligament injury.