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NCT ID: NCT06275087 Recruiting - Intraoral Tumor Clinical Trials

Differences in Speed of Recovery From Anesthesia for Intraoral Surgery

PSIOS
Start date: April 10, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare two groups of patients going in general anesthesia for intraoral surgery, the first group TIVA with propofol and the second group inhalational with sevoflurane. The main questions it aims to answer are to asses speed and quality of recovery from general anesthesia. Participants will fill out a questionnaire to evaluate the quality of recovery from anesthesia using the QoR-40 1h, 24h, and 30 days after waking up from anesthesia in comparison to the results of the same questionnaire before surgery. Also, the investigators will perform a hand grip and bite strength test on the patients after waking up from anesthesia in the operating room, after 1 hour in the recovery room, and after 24 hours compared to preoperative values. The investigators will compare TIVA and Volatile groups to see if there are any differences in recovery seed, muscle strength recovery, postoperative nausea and vomiting, and shivering between groups.

NCT ID: NCT06275815 Recruiting - Clinical trials for Developmental Language Disorder

Promoting Caregiver Implementation of an Effective Early Learning Intervention

Start date: April 10, 2024
Phase: N/A
Study type: Interventional

The goal of this study is to examine the impact of a caregiver-implemented shared reading program, Sit Together and Read (STAR), on children ages 4 to 5 with developmental language disorder. The main questions it aims to answer are: - how much STAR impacts children's literacy skills in the short-term and long-term--up to two-years after completing STAR. - how do caregiver supports in the form of small monetary rewards or encouraging texts help caregivers to implement STAR at its intended frequency of sessions per week. Caregiver participants will be assigned to either a control group or one of three STAR groups. Children's skills related to literacy and learning will be assessed before the intervention starts, at the end of the intervention, and every six months post-intervention for two years. Researchers will determine the short term and long term impacts of STAR compared to the control group. Researchers will compare the three STAR conditions to see if the rewards or encouragement helped parents to follow through with completing more STAR sessions.

NCT ID: NCT06277596 Recruiting - Fibromyalgia Clinical Trials

The Effects of Progressive Clinical Pilates Exercises Applied as 2 Different Ways in Fibromyalgia

Start date: April 10, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effects of progressive clinical Pilates exercises applied as group under the supervision of a physiotherapist and home exercise programs on pain level, physical condition, functional status, psychosocial status and quality of life in individuals with fibromyalgia between the ages of 20-50.

NCT ID: NCT06286748 Recruiting - Clinical trials for Chronic Kidney Diseases

Beetroot Extract Supplementation Associated With an Exercise Protocol for Chronic Kidney Disease Patients

Start date: April 10, 2024
Phase: N/A
Study type: Interventional

Chronic kidney disease (CKD) patients often present systemic inflammation and oxidative stress, resulting in metabolic disorders and high rates of disease-associated cardiovascular death. The literature has indicated that dietary control, the use of bioactive compounds, and the practice of regular physical exercise are essential for the prevention and management of CKD and its complications. In this context, beetroot (Beta vulgaris rubra) deserves attention as it is a source of several bioactive compounds, such as nitrate, betaine, and betalain, with beneficial effects for CKD patients, including anti-inflammatory, antioxidant effects, reduction of blood pressure, and vasodilatory action. The antioxidant and anti-inflammatory properties, in addition to their vasodilatory and antihypertensive capacity, can make supplementation of beetroot an excellent nutritional strategy to help in the treatment of CKD patients. So, this research project will bring contributions to the scientific world, providing strategies for application in clinical practice and the care of patients with CKD, on the use of beetroot associated with an exercise protocol as a non-pharmacological strategy in modulating inflammation, oxidative stress, and improved functional capacity. Furthermore, when supplemented hours before physical training, has been identified as an important factor in improving performance in these activities. Therefore, this study aims to evaluate the effects of supplementation (acute and chronic) of beetroot extract associated with an exercise protocol on complications associated with CKD.

NCT ID: NCT06296043 Recruiting - Clinical trials for Premenstrual Syndrome

The Effect of Su-Jok Application and Progressive Muscle Relaxation Exercises in Coping With Premenstrual Syndrome

Start date: April 10, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effect of su-jok application and progressive muscle relaxation exercise in coping with premenstrual syndrome.

NCT ID: NCT06307431 Recruiting - Clinical trials for Renal Cell Carcinoma

A Study of Adjuvant V940 and Pembrolizumab in Renal Cell Carcinoma (V940-004)

Start date: April 10, 2024
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to compare V940 plus pembrolizumab to placebo plus pembrolizumab with respect to disease-free survival (DFS) as assessed by the investigator. The primary hypothesis is that V940 plus pembrolizumab is superior to placebo plus pembrolizumab with respect to DFS.

NCT ID: NCT06309121 Recruiting - Obesity, Childhood Clinical Trials

Effects of the Postbiotic Blend ABB C3 on Adiposity and Glucose Metabolism in Children and Adolescents

PostOb
Start date: April 10, 2024
Phase: N/A
Study type: Interventional

This study investigates the effects of a postbiotic combination called ABB C3 on reducing body fat and improving metabolic health in children and teenagers. The study consists of a 3-month trial with half participants taking ABB C3 and the other half a placebo, monitoring body composition and blood markers. Afterward, participants can continue with ABB C3 for an additional 3 months. The goal is to determine if ABB C3 is a safe and effective way to help young people improve their health by reducing body fat.

NCT ID: NCT06311578 Recruiting - Clinical trials for Advanced Solid Tumors

A Study of JNJ-87704916, as Monotherapy and in Combination for Advanced Solid Tumors

Start date: April 10, 2024
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety, feasibility, recommended dose(s) and regimen(s) of JNJ-87704916 as monotherapy and in combination with cetrelimab.

NCT ID: NCT06313541 Recruiting - NSCLC Stage IV Clinical Trials

Treatment Response Adapted Hybrid Radiotherapy in Metastatic Non-small Cell Lung Cancer Receiving First-line Immunotherapy

Start date: April 10, 2024
Phase: Phase 2
Study type: Interventional

This study is a multicenter, randomized controlled clinical trial to explore the preliminary efficacy and safety of treatment response adapted hybrid radiotherapy (LDRT and SBRT) in the first-line treatment of immunotherapy combined with chemotherapy for advanced driver-gene negative NSCLC, and to provide new ideas for the comprehensive treatment of advanced NSCLC

NCT ID: NCT06314256 Recruiting - Clinical trials for Interdental Papilla Loss

Clinical Evaluation of Hyaluronic Acid and Platelet Rich Fibrin Injection Efficacy in Interdental Papilla Reconstruction

Start date: April 10, 2024
Phase: Phase 4
Study type: Interventional

The goal of this clinical trial is to evaluate and compare the efficacy of injectable platelet rich fibrin (i-PRF) and hyaluronic acid (HA) in reconstruction of interdental papilla loss. The main questions it aims to answer are: - How compareable are above mentioned two interventions (i-PRF&HA) in reconstruction of interdental papilla loss? - Which treatment option is better accepted by patients? Which treatment option would patients be more satisfied with? Participants with multiple interdental papilla loss will be treated with both i-PRF and HA in split-mouth design. Researchers will compare two treatment options to see if black triangles caused by interdental papilla loss closes and if yes, for how long do they last.