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NCT ID: NCT04250701 Completed - Clinical trials for Intellectual Disability

Postural Control, Grip Strength and Body Posture in Children With Intellectual Disability and Dyslexia

Start date: February 15, 2017
Phase:
Study type: Observational

This study investigates physical changes in children with Dyslexia and Intellectual Disability. Participants divided into three groups and Body Posture, Postural Control and Hand Grip Strengths was evaluated.

NCT ID: NCT04250129 Recruiting - Sentinel Lymph Node Clinical Trials

SENTINEL LYMPH NODE BIOPSY AFTER NEOADJUVANT CHEMOTHERAPY

NEOSENTITURK
Start date: January 31, 2018
Phase:
Study type: Observational

Omitting axilary lymph node dissection (ALND) following SLNB with residual cancer in patients with locally advanced disease after neoadjuvan chemotherapy (NAC) is still controversial. In this study, the investigators evaluated factors affecting local recurrence and outcome in patients with locally advanced breast cancer (LABC), who underwent sentinel lymph node (SLN) with or without ALND after NAC.

NCT ID: NCT04249765 Recruiting - Hand Grasp Clinical Trials

Hand Strength And Hand-Reaction Parameters Of Post Millennial: An Example Of Students' Group In Central Anatolia

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

The aim of this research is to find out whether there exists a correlation between such important characteristic of individual's hand performance as grip strength, pinch strength, and the hand reaction. In addition, it will be investigated whether there is a change in normative values of this age group in relation to modern lifestyle. The study includes statistical data analysis and interpretation of the derived outcomes.

NCT ID: NCT04248829 Active, not recruiting - Clinical trials for Non-Small Cell Lung Cancer

Clinical Trial of YH25448(Lazertinib) as the First-line Treatment in Patients With EGFR Mutation Positive Locally Advanced or Metastatic NSCLC (LASER301)

Start date: February 13, 2020
Phase: Phase 3
Study type: Interventional

This Phase III study will be conducted to evaluate the efficacy and safety of YH25448 as first-line treatment in locally advanced or metastatic Non-small Cell Lung Cancer (NSCLC) patients with EGFR mutations

NCT ID: NCT04248764 Completed - Muscle Soreness Clinical Trials

Investigating the Effects of Different Soft Tissue Mobilizations on Delayed Onset Muscle Soreness

Start date: February 10, 2021
Phase: N/A
Study type: Interventional

Delayed onset muscle soreness (DOMS) is associated with the initiation of a new physical activity or a sudden increase in exercise volume and intensity. DOMS also occurs following eccentric exercises such as ballistic stretching, downhill running, weight training and plyometrics. DOMS might prevent performing sports and decreases the performance of professional or recreational athletes. Recently, different soft tissue mobilization applications (massage, foam roller) have been preferred by many athletes to prevent DOMS. However, there is no study comparing the effects of these techniques on DOMS. Therefore, the aim of the present study is to investigate the effects of different soft tissue mobilization practices on DOMS and sportive performance in recreational athletes. In order to achieve this goal, a total of 36 recreational athletes will be included and will be allocated to three groups as foam roller group (n=12), massage group (n=12) and control group (n=12). Demographic data, thermal camera measurements, fatigue level assessments, and performance measurements will be performed. All measurements will be carried out four times as before the application, immediately after the application, after 24 hours and after 48 hours.

NCT ID: NCT04248660 Completed - Pregnancy Related Clinical Trials

Uterine Artery Doppler and 11-14 / 20-22 Weeks of Gestation Pregnancy

Start date: January 1, 2016
Phase:
Study type: Observational

Uterine artery doppler measurements will be made at 11-14 weeks and 20-22 weeks of gestation, and the classification of these measurements according to type of delivery; and to investigate the change in the effect of delivery type on uterine artery flows on obstetric outcomes (maternal, fetal, neonatal outcomes).

NCT ID: NCT04248478 Recruiting - Fibromyalgia Clinical Trials

Eating Behaviours in Female Patients With Fibromyalgia

Start date: January 29, 2020
Phase:
Study type: Observational

The Relationship Between Eating Behaviours and Health Status of Female Patients with Fibromyalgia

NCT ID: NCT04247789 Completed - Fatigue Clinical Trials

The Associated Factors With Fatigue in Older Adults Living in a Rest Home

Start date: December 23, 2019
Phase:
Study type: Observational

Fatigue is an important and prevalent problem in older adults. The ratio of fatigue may rise in older adults who live in nursing homes/rest homes. In the literature, a few studies investigated the prevalence of fatigue, and there is no study explaining the associated factors. The aim of the present study is to investigate the prevalence of fatigue in rest home residents and to determine the associated variables with fatigue.

NCT ID: NCT04246567 Suspended - Hypoxia Clinical Trials

Evaluation of the Effect of Sevoflurane and Propofol Hypotensive Anesthesia on Blood Antioxidant Levels and HIF 1 Levels

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study to evaluate the patients who underwent controlled hypotensive anesthesia under standardized depth of anesthesia with total intravenous anesthesia or inhalation anesthesia; preoperative and 30. ,60. ,120. second of intraoperative period blood HIF 1a, TAS, TOS measurement and to investigate tissue hypoxia secondary to hypotensive anesthesia and the changes of the mediators at the tissue level and which hypotensive anesthesia technique is related.

NCT ID: NCT04246255 Completed - Local Anesthesia Clinical Trials

Pain Relief During Intravenous Cannulation in Pediatric Patients

Start date: February 3, 2020
Phase: Phase 4
Study type: Interventional

Performing intravenous (IV) cannulation to pediatric patients might be much harder than adult ones according to their anxiety levels. However, managing adult patients during intravenous cannulation is also challenging if he or she had a noxious memory about the situation or has a low pain threshold. Therefore, it is essential to relieve the pain of an IV needle or an IV cannula insertion in the pediatric patient population. Lidocaine Hcl spray (Xylocaine 10% Oral ) will be utilized to the research group, and Serum Physiologic (Serum Fizyolojik %0,9 10 ml ampule, Biofarma İlaç San. ve Tic A.Ş., İstanbul, Turkey) will be utilized to the control group of the study. Both medications will be administrated by spraying the formula three times to an adhesive bandage and placing it to the skin that IV cannulation will be performed. After waiting for a minimum of 5 to a maximum of 15 minutes ( waiting time is closely associated with the patient's anxiety level), IV cannulation will be performed from the same area by an experienced pediatric nurse. The investigator hypothesizes that utilizing the spray form of the Lidocaine Hcl formula to the skin with an adhesive bandage before IV cannulation might lower the pain of the manipulation in pediatric patients, which might cause lower anxiety levels with stable vital signs.