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Syndrome clinical trials

View clinical trials related to Syndrome.

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NCT ID: NCT05578469 Active, not recruiting - Marfan Syndrome Clinical Trials

Surgical Treatment of Marfan Syndrome With Subluxation Lens

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

To analyze the postoperative visual effects, and to compare the safety and efficacy of different surgical treatment with of Marfan Syndrome with subluxation lens.

NCT ID: NCT05556733 Active, not recruiting - COVID-19 Clinical Trials

FMT for Post-acute COVID-19 Syndrome

FMT-PACS
Start date: September 28, 2022
Phase: N/A
Study type: Interventional

In recovered COVID-19 patients, emerging global data have reported the presence of long COVID, that is, at least one symptom that an alternative diagnosis cannot explain has been persistent for four or more weeks after the initial infection. We demonstrated previously that almost 80% of recovered COVID-19 patients in Hong Kong suffer from Long COVID for more than 6 months, affecting multiple body systems. In a recent study, the five most common Long COVID symptoms were fatigue, memory problem, difficulty sleeping, anxiety and hair loss. One promising hypothesis is the involvement of the gut microbiota, a collection of the trillions of gut microorganisms that play important immunomodulatory roles against infections. Faecal microbiota transplantation (FMT), which is the infusion of processed faeces from healthy donors to the gut of affected subjects, has shown impressive therapeutic effects for recurrent Clostridioides difficile infection and other emerging indications. Gut microorganisms together with the metabolites in the donated faeces could potentially modulate the gut microbiota of the recipient and treat the dysbiosis associated with pathological health conditions. To date, no study has yet to assess the therapeutic effects of FMT in post-COVID-19 neuropsychiatric conditions.

NCT ID: NCT05548738 Active, not recruiting - Clinical trials for Chronic Pain Syndrome

Caudal Epidural Prolotherapy Versus Steroids in Failed Back Surgery Syndrome

Start date: April 20, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

This study will be held on patients with failed back surgery syndrome, the investigators are comparing prolotherapy and steroids injections in caudal epidural space to relieve the pain

NCT ID: NCT05543408 Active, not recruiting - COVID-19 Clinical Trials

Long COVID-19 Syndrome in Primary Care: A Novel Protocol of Exercise Intervention "CON-VIDA Clinical Trial"

CON-VIDA
Start date: May 3, 2022
Phase: N/A
Study type: Interventional

This is a randomized controlled trial of the efficacy of an individualized, progressive, exercise program (strength, cardiovascular, and breathing exercises) in recovering people from the post-COVID-19 syndrome (i.e., patients who present symptoms >12 weeks once the acute phase of the disease is over).

NCT ID: NCT05543174 Active, not recruiting - Clinical trials for Alagille Syndrome (ALGS)

A Study of TAK-625 for the Treatment of Alagille Syndrome (ALGS)

Start date: January 16, 2023
Phase: Phase 3
Study type: Interventional

The main aim of the study is to check if TAK-625 improves symptoms of Alagille Syndrome (ALGS), side effect from the study treatment or TAK-625, and how much TAK-625 stays in their blood over time. This will help the study sponsor (Takeda) to work out the best dose to give people in the future. The participants will be treated with TAK-625 for up to the end of study (about 34 months). Participants will visit their study clinic 9 times from the start of study. After 9 times visits, participants will visit their study clinic every 12 weeks up to the end of study.

NCT ID: NCT05532423 Active, not recruiting - Metabolic Syndrome Clinical Trials

Nitrate Supplementation and Cerebrovascular and Cognitive Function in Metabolic Syndrome

Start date: December 1, 2022
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to determine if beetroot juice consumption can improve cognitive performance and brain vascular function in individuals with metabolic syndrome

NCT ID: NCT05529108 Active, not recruiting - Diabetes Clinical Trials

Glycaemic Control Effect of BSG and Underlying Gut - Related Mechanism in Singapore Adults With Metabolic Syndrome

Start date: October 28, 2022
Phase: N/A
Study type: Interventional

The purpose of this research project is to assess the glycaemic controlling effects of consuming BSG and bio-transformed BSG-containing biscuits and its underlying gut - related mechanism in adults with MetS using in-vivo setting.

NCT ID: NCT05520086 Active, not recruiting - Clinical trials for Stevens-Johnson Syndrome

Clinical Trial to Evaluate Safety and Efficacy of Cell Therapy in Patients With Cicatricial Conjuntivitis.

CELOPHIN
Start date: November 11, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

A phase IIa, open label, non controlled clinical trial to assess the feasibility and safety of allogeneic adipose-derived mesenchymal stem cells (ASC) in the treatment of cicatricial conjunctivitis associated with Lyell's syndrome, Stevens-Johnson's syndrome and mucous membrane pemphigoid with ocular involvement

NCT ID: NCT05495074 Active, not recruiting - Metabolic Syndrome Clinical Trials

Design of a Genetic Score to Predict the Response to a Dietary Intervention in Adults With Metabolic Syndrome

Start date: September 2, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate whether a genetic score based on genetic variants related to amino acid metabolism could predict the response to a dietary intervention in adults with metabolic syndrome.

NCT ID: NCT05490446 Active, not recruiting - Clinical trials for Myelodysplastic Syndromes

A Study of AG-946 in Participants With Anemia Due to Lower-Risk Myelodysplastic Syndromes (LR-MDS)

Start date: November 7, 2022
Phase: Phase 2
Study type: Interventional

This purpose of this study is to establish proof of concept of AG-946 in participants with LR-MDS in Phase 2a and to compare the effect of AG-946 versus placebo and to detect a dose response for erythroid response in participants with LR-MDS in Phase 2b.