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NCT ID: NCT06001034 Completed - Fibromyalgia Clinical Trials

Program of Supervised Occlusive Aerobic Training in People With Fibromyalgia.

Start date: September 15, 2022
Phase: N/A
Study type: Interventional

Occlusive training in people with fibromyalgia

NCT ID: NCT05998499 Completed - HIV-1-infection Clinical Trials

HIV-Infected Latin American Asylum Seekers in Europe: Insights From the EuroLatin HIV Cohort

ELHC
Start date: January 30, 2022
Phase:
Study type: Observational [Patient Registry]

This is a longitudinal observational study conducted in Europe that describes migrants infected with HIV from Latin America who come to Europe with the intention of seeking asylum or international protection. The aim of the study is to identify the barriers this population faces in accessing the healthcare system and to assess disease control

NCT ID: NCT05995314 Completed - Caffeine Clinical Trials

Effects Of Caffeine On Cognitive Performance

Start date: August 7, 2023
Phase: N/A
Study type: Interventional

Caffeine is a potent central nervous system stimulant that increases the activity in the prefrontal cortex and can improve cognitive skills. An improvement in these cognitive skills can lead to further benefits in athletic performance. Therefore, it is necessary to clarify the dose-response of caffeine on cognitive performance.The aim of this research will be to determine the effects of different doses of caffeine on sport-related cognitive aspects.

NCT ID: NCT05994560 Completed - Uterine Myomectomy Clinical Trials

The Value of Uterine Artery Occlusion in Laparoscopic Myomectomy

Start date: March 2, 2020
Phase: N/A
Study type: Interventional

The objective of this study is to determine whether patients undergoing laparoscopic myomectomy with temporary occlusion of the uterine arteries and utero-ovarian ligaments using clips experience a decrease in blood loss during surgery compared to patients who undergo laparoscopic myomectomy without clips.

NCT ID: NCT05994469 Completed - Groin Injury Clinical Trials

Prevention of Groin Injuries in Rink Hockey

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

Rink hockey teams from senior category (adults) will be recruited to implement a groin injury prevention program consisting on the Copenhagen Adduction Exercise (CAE) throughout the regular season, 0 times, once or twice per week (september 2023-march 2024) Weekly team exposure to training sessions and games will be collected as well as cases of groin problems in the entire population When the season ends, the number of groin problems will be compared between teams that used the prevention program once a week against twice a week or no sessions a week.

NCT ID: NCT05993377 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Prediction of Duration of Mechanical Ventilation in ARDS

PIONEER
Start date: August 14, 2023
Phase:
Study type: Observational

The investigators are planning to perform a secondary analysis of an academic dataset of 1,303 patients with moderate-to-severe acute respiratory distress syndrome (ARDS) included in several published cohorts (NCT00736892, NCT022288949, NCT02836444, NCT03145974), aimed to characterize the best early scenario during the first three days of diagnosis to predict duration of mechanical ventilation in the intensive care unit (ICU) using supervised machine learning (ML) approaches.

NCT ID: NCT05991141 Completed - Pain Clinical Trials

Could Apnea Induce Hypoalgesia?

Start date: February 1, 2023
Phase: N/A
Study type: Interventional

A randomized controlled trial (RCT) in healthy subjects will be conducted with the following aims: (1) Explore the effect of low pulmonary volume dynamic apnoea bouts on Pressure Pain Threshold (PPT) and conditioned pain modulation (CPM); (2) analyse whether CPM response correlates with apnoea induced hypoalgesia; (3) examine the association between apnoea bouts, Rate of Perceived Exertion, hypoxemia and Heart Rate changes in PPT.

NCT ID: NCT05989295 Completed - Children Clinical Trials

A Probiotic That Reduces Atopic Skin

Start date: January 26, 2022
Phase: N/A
Study type: Interventional

To assess the efficacy and safety of the use of probiotics as food supplements in reducing the SCORAD index in children with atopic skin compared with placebo. This is a randomized, placebo-controlled, double-blind clinical trial with 2 parallel groups, which will include 32 patients who attend some of the research centers. Patients will be randomized into one of the 2 study groups (allocation ratio 1: 1): Experimental group (Lactobacillus rhamnosus LRa05) and placebo group (placebo). The reduction of the SCORAD index, the number of sprouts in 12 weeks, the days of use of topical corticosteroids and one valuations of the skin condition (hydration).

NCT ID: NCT05988580 Completed - Clinical trials for Postprandial Glycemia

Postprandial Glycemia After Eating a Pasta Dish Made With Resistant Starch.

ALISSEC2
Start date: September 1, 2023
Phase: N/A
Study type: Interventional

Resistant starch partially resists hydrolyzation by digestive enzymes in humans. Consequently, it is not absorbed in the small intestine and goes directly to the large intestine, where it is fermented by the intestinal microbiota, acting as a prebiotic and stimulating the growth of beneficial bacteria in the colon. In addition, the effect of resistant starch on postprandial glucose metabolism is studying. Thus, the present research on healthy subjects has been proposed. The main objective is to assess the effect on postprandial glycemia of eating a pasta dish made with resistant starch versus its original version. For this purpose, a randomized, double blind crossover study has been designed. Target sample size is 18 subjects.

NCT ID: NCT05987878 Completed - Clinical trials for Strabismus, Comitant

Single Minimal Conjunctival Incision for Strabismus

Start date: January 31, 2021
Phase:
Study type: Observational

The purpose of this investigation is to study the feasibility and inflammatory response of surgery for rectus muscles using a small single bulbar conjunctival incision posterior and parallel to the muscle insertion. Patients requiring surgery of at least one rectus muscle with several diagnoses, operated under general or topical / sub-Tenon's anesthesia, who had no previous eye muscle surgery, will be recruited. Routinary clinical ophthalmological examination will be carried out. After applying a 5-0 PGA traction suture, a 3-4 mm single conjunctival incision posterior and parallel to the rectus muscle insertion will be done. A hang-back recession with 6-0 PGA suture will be carried out, and the conjunctiva closed by an 8-0 PGA single stitch. The main outcome measure will be duration of swelling and hemorrhage, and secondary outcome measure will be motor outcome at 2 months after surgery.