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NCT ID: NCT05896748 Completed - Clinical trials for Human Immunodeficiency Virus Type 1 (HIV-1)

Study to Assess the Effects of Cabotegravir (CAB) and Rilpivirine (RPV) Long-Acting (LA) Injections Following Sub-cutaneous (SC) Administration Compared With Intramuscular (IM) Administration in Adult Participants Living With Human Immunodeficiency Virus (HIV-1) Infection in the FLAIR Study

Start date: November 8, 2022
Phase: Phase 3
Study type: Interventional

This study will assess the pharmacokinetics, safety, tolerability, maintenance of virological suppression and patient reported outcomes for participants receiving CAB and RPV LA injections following SC administration in the anterior abdominal wall SC tissue compared with IM administration in the gluteus medius muscle in adult participants living with HIV-1 infection in the FLAIR study (NCT02938520).

NCT ID: NCT05895734 Completed - Multiple Sclerosis Clinical Trials

Effectiveness of Powerball System in People With Multiple Sclerosis

EMPOW
Start date: January 10, 2023
Phase: N/A
Study type: Interventional

There is a high percentage of impairment in the upper limbs (UL) in patients with multiple sclerosis (MS), being muscle strength and hand dexterity a determining factor for the preservation of functional activities, constituting the basis of independence and quality of life. The aim of this study is to determine the effects of a training protocol on UL muscle strength, through the NDS-Powerball® system, in combination with conventional physiotherapy, during 8 weeks in terms of muscle strength, coordination, fatigue, functionality and quality of life in people with MS.

NCT ID: NCT05893251 Completed - Clinical trials for Temporomandibular Joint Dysfunction Syndrome

Effectiveness of Cervical Treatment in Wind Musicians With Temporomandibular Dysfunction

ANAISATM
Start date: November 1, 2017
Phase: N/A
Study type: Interventional

Temporomandibular dysfunction (TMD) consists of a series of multifactorial signs and symptoms that occur in the orofacial region, with pain being the most common symptom. There is a close biomechanical and anatomical relationship between the cervical region and the temporomandibular joint (TMJ) through the trigemino-spinal nucleus. Objectives: To comparatively assess the improvement in subjects with TMD when adding cervical manual therapy to a postural treatment. Additionally, to determine if both cervical treatments separately produce changes in the TMJ. Materials and methods: An experimental study of randomized controlled clinical trial type was conducted. The study involved 30 wind instrument players randomly assigned to an experimental group (EG) and a control group (CG). After obtaining consent, measurements were taken for maximum mouth opening (MMO), cervical range of motion, and pain threshold to pressure (PTP) in the masseter and temporalis muscles. Both groups underwent active cervical postural treatment for 4 weeks, and the EG additionally received a cervical manual therapy protocol. An initial assessment was conducted before the intervention, and a final assessment was done one week after the last intervention. The statistical program SPSS was used for data analysis.

NCT ID: NCT05892835 Completed - Sports Accident Clinical Trials

Attitude and Knowledge of Basic Life Support of Professional Soccer Players and Coaches in Valencian Community

RCPVIL
Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Aim Given the increasing occurrence of cases of cardiorespiratory arrest on soccer fields around the world, it seems pertinent to find out the degree of training and the attitude shown by the players and coaches themselves. The objective was to measure the knowledge and attitude of soccer professionals before and after a training intervention. Method After an exhaustive bibliographic review, a series of questions have been analyzed and selected, with which an ad hoc questionnaire has been prepared. This questionnaire has been completed by soccer players from the Spanish first division, male and female teams and their coaches. Once the data was collected, a training workshop was carried out to improve both the attitude and knowledge in relation to cardiopulmonary resuscitation (CPR).

NCT ID: NCT05888753 Completed - Outcome Assessment Clinical Trials

Textbook Outcome in Adrenal Neoplasms

Start date: September 1, 2022
Phase:
Study type: Observational

BACKGROUND: Textbook outcome (TO) is a multidimensional quality management tool that uses a set of traditional surgical measures to reflect an "ideal" surgical result for a particular pathology. The aim of the present study is to record the rate of TO in patients undergoing elective surgery for adrenal neoplasms. MATERIAL AND METHODS: Retrospective study of all patients undergoing scheduled adrenal neoplasms surgery at a Spanish university hospital from September January 2010 to December 2022. Emergency surgeries were excluded. The variables included in the definition of TO were: R0 resection, no Clavien-Dindo ≥IIIa complications, no prolonged stay, no readmissions, and no mortality in the first 30 days. The main objective of this study is to analyse the achievement of TO in a series of patients undergoing scheduled adrenal neoplasms resection at the Doctor Balmis General University Hospital in Alicante, Spain. The investigators compare the group of patients who achieve a TO result with the group of patients who do not. A univariable and multivariable analysis will be carry out in order to indentified the variables associated with TO.

NCT ID: NCT05888116 Completed - Vaginal Disease Clinical Trials

Efficacy and Safety of a Hyaluronic Acid-Based Vaginal Moisturizer Medical Device to Ease Symptoms of Vaginal Dryness

HYALU-LAUDE
Start date: May 23, 2023
Phase: N/A
Study type: Interventional

This study evaluates the efficacy and safety of a new hyaluronic acid-based vaginal moisturizer gel to ease symptoms of vaginal dryness compared to a commonly used marketed vaginal moisturizer (Cumluade Hidratante Interno®).

NCT ID: NCT05885945 Completed - Clinical trials for Dysmenorrhea Primary

Diaphragmmatic Muscle Strength and Balance in Women With Dysmenorhea

Dysmenorhea
Start date: February 15, 2023
Phase:
Study type: Observational

Analysis of stabilometric and respiratory variables in patients with dysmenorrhea during the first day of the menstrual cycle and any other day outside the cycle.

NCT ID: NCT05884424 Completed - Dementia Clinical Trials

Effectiveness and Cost-Effectiveness of Robot Therapy With the Paro Robot in People Living With Dementia

Start date: April 10, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and cost-effectiveness of group robot therapy with the PARO therapy robot in terms of quality of life and neuropsychiatric symptoms in people living with dementia in residential centers. In addition, the acceptability of the robot on the part of the users participating in the study will be evaluated. The evaluation will be carried out through a multicenter pragmatic clinical trial randomized to an intervention group (PARO therapy robot) or a control group (treatment as usual). Participants in the intervention group will complete three sessions per week with the PARO therapy robot during 12 weeks. Participants in the control group will maintain their standard care. In addition, a follow-up evaluation will be made three months after the end of the intervention to assess the duration of the possible effects.

NCT ID: NCT05880186 Completed - Dietary Supplement Clinical Trials

Influence of the Time of Day in the Effect of Caffeine on Maximal Fat Oxidation During Exercise in Women

CIRCAF_WOM
Start date: February 9, 2021
Phase: N/A
Study type: Interventional

Caffeine is a natural stimulant with well-recognized metabolic benefits, however, there is a lack of studies investigating the time-of-day caffeine influence to enhance fat oxidation in women. The aim of this study was to evaluate the influence of the time of the day on the effect of caffeine on maximal rate of fat oxidation during aerobic exercise in women.

NCT ID: NCT05879094 Completed - Healthy Subjects Clinical Trials

Orthopaedic Simulation of Morton's Extension to Test the Effect on Plantar Pressures of Each Metatarsal Head in Patients Without Deformity: A Pre-post-test Study.

Start date: May 29, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to simulate the orthopedic treatment called Morton's extension on non-deformed patients to check the effects on each metatarsal head on its static footprint.