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NCT ID: NCT04345523 Completed - COVID-19 Clinical Trials

Convalescent Plasma Therapy vs. SOC for the Treatment of COVID-19 in Hospitalized Patients

ConPlas-19
Start date: April 3, 2020
Phase: Phase 2
Study type: Interventional

A total of 278 patients are planned. All patients will be in an early-stage of COVID-19. They must be adults and hospitalized. In this study, all participating patients will receive the standard treatment provided according to the current treatment protocols for coronavirus disease. In addition to this treatment, each patient will be randomly assigned to receive additional treatment with convalescent plasma transfusion (CP; blood plasma from patients who have been cured of coronavirus), or continue with standard treatment but without adding transfusion. 50% of the chances of additional treatment with CP, and 50% of the chances of receiving only the standard treatment for coronavirus. The duration of the study shall be one month from the assignment of the treatment. The patient and the doctor will know the treatment assigned.

NCT ID: NCT04345367 Completed - Atopic Dermatitis Clinical Trials

Study of Abrocitinib Compared With Dupilumab in Adults With Moderate to Severe Atopic Dermatitis on Background Topical Therapy

Start date: June 11, 2020
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, double-dummy, active-controlled, multi-center study to assess the efficacy and safety of abrocitinib 200 mg (2 x 100 mg tablets) administered orally QD compared with dupilumab 300 mg administered by subcutaneous injection every other week (as per label guidelines) in adult participants on background topical therapy, with moderate to severe AD. The treatment duration is 26 weeks. A total of approximately 600 participants will be enrolled from approximately 220 sites globally. Approximately 600 participants will be randomly assigned to study intervention. There are primary efficacy assessments at Week 2 and Week 4, and a key secondary efficacy assessment at Week 16. Efficacy and safety endpoints will be assessed throughout the entire study. Exploratory endpoints related to hand eczema efficacy will be assessed throughout the study.

NCT ID: NCT04345237 Completed - Body Composition Clinical Trials

Changes in Body Composition When Ingesting a Dairy Compound Enriched With Leucine

LEUCI
Start date: November 15, 2019
Phase: N/A
Study type: Interventional

Controlled clinical trial, randomized by strata (sex and period of the study), with 6 parallel branches to the study depending on the type of product consumed and the type of physical exercise program performed, double-blind masked for the consumption of the product and single-center.

NCT ID: NCT04345211 Completed - Aging Clinical Trials

Manual Therapy, Thera-band Exercise and Walking

MTBEW
Start date: October 25, 2021
Phase: N/A
Study type: Interventional

Worldwide, the number of older adults is expected to more than double by 2050 and more than triple by 2100, with most of the increase in developing countries. This situation has become a challenge to health professions such as physical therapy, since aging involves a gradual reduction in the capacity to adapt and an increase in vulnerability to health issues such as chronic non-communicable diseases and musculoskeletal disorders. The respiratory system, as the rest of the body, is exposed to both physiological aging and disease. According to the World Health Organization , respiratory diseases such as trachea, bronchi, or lung cancer, lower respiratory tract infections, or chronic obstructive pulmonary disease are found in the third, fifth, and sixth cause of death, respectively, among the top ten. Therefore, bronchopulmonary and thoracic pathology constitutes an important problem for Public Health, both due to the high number of affected subjects and to their potential severity For this reason, the recommendations of the European, North American and national societies, highlight, among other aspects, the importance of the prevention of these diseases. They also insist on the need to maintain the integrity of the thoraco-abdominal anatomical elements and preventive treatment in those at risk, before symptoms appear. These recommendations together with the change of perspective that is being taken into account when treating aging have led to the fact that in the last decade more research has been started on the respiratory system in older people without respiratory problems. The aim of this trial is to investigate whether manual therapy, elastic band exercise or walking can mitigate the effects of age-related changes in lung function in adults over 60 years old. Also whether there is a difference in effect between the different forms of therapy.

NCT ID: NCT04345055 Completed - Hamstring Injury Clinical Trials

Immediate Impact of Lumbar Fascia Stretching on Hamstring Flexibility

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

Introduction: the hamstring muscles has a great tendency to decrease its extensibility, originating a pathology with a own clinical entity, the Short Hamstring Syndrome (SHS), in addition to other problems on adjacent structures. All this present a great socioeconomic impact in the investigator's society. Various techniques have been demostrated to prduce an increase in flexibility, among which are the fascial techniques. Objective: to evaluate the immediate efficacy of the treatment of the lumbar fascia in the flexibility of the hamstring musculature. Methods: 41 women between 18 and 39 years old, in two groups. The experimental group received a technique of fascial stretching in the lumbar area while the control group participated in an off magnetotherapy machine. The hamstring flexibility in both lower limbs was measured by the Straight Leg Raising Test (SLR) and the Passive Popliteal Angle Test (PKE).

NCT ID: NCT04345029 Completed - Clinical trials for Overweight and Obesity

Effectiveness of a Natural Ingredient on Appetite Regulation

SAC
Start date: January 15, 2020
Phase: N/A
Study type: Interventional

Single-center, double-blind, double-crossed, randomized controlled clinical trial with two crossed branches, designed with the objective of evaluating the effect of the investigational product on satiety.

NCT ID: NCT04344587 Completed - COVID-19 Clinical Trials

Awake Prone Position for Early Hypoxemia in COVID-19

APPEX-19
Start date: April 23, 2020
Phase: N/A
Study type: Interventional

Prone positioning is a well studied and validated treatment for severe acute respiratory distress syndrome (ARDS), however there are no randomized studies on the use of prone positioning in the non-intubated patient. It is unknown if this intervention would be helpful in preventing further respiratory deterioration in terms of increasing supplemental oxygen requirements, endotracheal intubation, and ICU admission. The Awake Prone Position for Early hypoxemia in COVID-19 (APPEX-19) Study is a pragmatic adaptive randomized controlled unblinded trial. APPEX-19 randomizes non-ICU patients with COVID-19 or who are under evaluation for COVID-19 to lie in a prone position (i.e, with their stomach and chest facing down) or to usual care.

NCT ID: NCT04344002 Completed - Covid-19 Clinical Trials

LunG and Melanoma canceR pAtients coVId19 Disease (GRAVID)

GRAVID
Start date: April 21, 2020
Phase:
Study type: Observational [Patient Registry]

This is a multi-centre study on lung cancer patients which experienced COVID-19. Information on clinical features, clinical course, management and outcomes will be collected for both, thoracic cancers and COVID-19 infection. Firstly, investigators will be registered in an online secure registry. After that, a protocol will be developed in order to collect clinical data for the research. It will also include I on the care organization or the perception of the patient and their family members. The final stage will consist on retrospective data collection from patients. So, it is a retrospective study data collection, preceded by prospective data registry.

NCT ID: NCT04343833 Completed - Clinical trials for Immediate Dental Implant

Immediate Implants in the Aesthetic Zone

Start date: October 2, 2017
Phase: N/A
Study type: Interventional

The use of immediate implants in the aesthetic area is a technique widely used in modern implantology. The characteristics of the patient, the implant, and the surgical procedure used may influence the final results. The aim was to assess whether the implant design affects primary (PS) and secondary stability (SS), bone level (BL), and PES/WES evaluation.

NCT ID: NCT04343599 Completed - Muscle Weakness Clinical Trials

Hypopressive Effectiveness in Postural Control and Pelvic Floor.

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

Effects of an exercise program based on hypopressive exercises in the female population.