Clinical Trials Logo

Filter by:
NCT ID: NCT05960890 Recruiting - Heart Failure Clinical Trials

Cohort Study of Chronic Heart Failure

CHF
Start date: June 8, 2023
Phase:
Study type: Observational

The goal of this observational study is to learn about the influencing factors of chronic heart failure prognosis in heart failure patients. The main question it aims to answer is that what are the influencing factors of clinical outcomes in chronic heart failure. Participants will be collected multiple omics data such as phenotype group, environmental exposure group, intestinal microbiome, genome, metabolome, and noninvasive biomarkers.

NCT ID: NCT05960721 Recruiting - Atrial Fibrillation Clinical Trials

Low-dose NOAC Versus GDMT After LAAO

RECORD-III
Start date: July 6, 2023
Phase: N/A
Study type: Interventional

The increased risk of Atrial fibrillation (AF) regarding thromboembolic stroke is predominantly due to the formation and embolization of clots from within the left atrial appendage (LAA). Percutaneous left atrial appendage occlusion (LAAO) is a nonpharmacological strategy for stroke prevention in patients with AF. Data from randomized trials, including PROTECT-AF, PREVAIL, and Prague-17, have suggested that LAAO has comparable efficacy to warfarin or NOACs. Considering these results, LAAO was recommended by the American College of Cardiology (ACC) and European Society of Cardiology (ESC) guidelines as a non-pharmacological stroke prevention strategy for patients with NVAF who have contraindications or are unsuitable for OAC. The PROTECT-AF and PREVAIL trials stipulated the use of standardized antithrombotic medications which were designed to minimize the risk of stroke, systemic embolism, or device-related thrombosis. This antithrombotic strategy was subsequently endorsed by the guidelines, briefly, patients with LAAO were discharged on warfarin and aspirin for 45 days post-LAAO, if there was no leak or a leak ≤5 mm under transesophageal echocardiography (TEE) at 45-day follow-up, antithrombotic strategies shall switch to dual antiplatelet therapy (DAPT) until 6 months post-LAAO, and then aspirin thereafter. Although LAAO was recommended by medical societies, previous patient-level meta-analyses have implied that compared with oral anticoagulation, LAAO had significantly more ischemic strokes, suggesting the inability of LAAO to prevent an ischemic stroke from sources beyond LAA. Will a combined strategy of LAAO and OAC further reduce the risk of stroke? The investigators hypothesized that a long-term low dose-Rivaroxaban (10mg daily) post-LAAO might be a potent supplement to the residue risk of ischemic stroke.

NCT ID: NCT05960617 Recruiting - Clinical trials for Glycogen Storage Disease Type IB

Efficacy and Safety of Empagliflozin in GSD-Ib Patients

Start date: July 15, 2023
Phase: Phase 2
Study type: Interventional

Empagliflozin Treatment of GSD-1b patients

NCT ID: NCT05960552 Recruiting - Clinical trials for Transesophageal Echocardiography

Perioperative Rescue Transesophageal Echocardiography in Intensive and Critical Status

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

We initiate this study to assess the diagnostic efficiency of PReTEE, a simplified TEE scan sequence with a combination of 3 valuable views of ME 4C, ME AV LAX and TG SAX, in identifying cardiac pathologies in the phase of difficult cardiopulmonary bypass separation among patients who will undergo high-risk cardiac surgical procedures.

NCT ID: NCT05959941 Recruiting - Healthy Clinical Trials

A Study of Macitentan in Healthy Chinese Adult Male Participants

Start date: July 5, 2023
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess what macitentan and its active metabolite (aprocitentan) does to the body after single dose administration of macitentan in Chinese healthy adult male participants.

NCT ID: NCT05959863 Recruiting - Clinical trials for Primary Aldosteronism

Primary Aldosteronism LC-MS/MS-specific Cutoffs

PM
Start date: August 30, 2023
Phase:
Study type: Observational

Aims to evaluation the LC-MS/MS-specific cutoffs of PA screening and CCT test.

NCT ID: NCT05959694 Recruiting - Clinical trials for Chronic Lymphocytic Leukemia

A Clinical Trial on the Safety and Efficacy of TQB3909 Tablets in Patients With Recurrent or Refractory Chronic Lymphocytic Leukemia (CLL) /Small Lymphocytic Lymphoma (SLL) .

Start date: October 11, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

This is a phase Ib/II clinical trial to evaluate the safety and efficacy of TQB3909 tablets in patients with recurrent or refractory CLL/SLL.

NCT ID: NCT05959356 Recruiting - Clinical trials for Metastatic Colorectal Cancer

Cetuximab and Envafolimab Plus mFOLFOXIRI as First-line Treatment for RAS/BRAF Wild-type, MSS, Unresectable Left-side Metastatic Colorectal Cancer

CEIL
Start date: November 9, 2023
Phase: Phase 2
Study type: Interventional

The primary aim of phase II CEIL study is to evaluate the efficacy of cetuximab and envafolimab plus mFOLFOXIRI versus cetuximab plus mFOLFOX6/FOLFIRI as first line treatment of patients with initially unresectable and previously untreated RAS/BRAF wild-type, MSS, left-side metastatic colorectal cancer(mCRC), in terms of Progression-free Survival.

NCT ID: NCT05958901 Recruiting - Clinical trials for Pulmonary Hypertension

Pulmonary Hypertension Observational Study

Start date: July 12, 2023
Phase:
Study type: Observational

The purpose of this study is to establish the large PH cohort and biological database in China, aiming for precision medicine to optimize diagnosis and treatment choices.

NCT ID: NCT05958719 Recruiting - Clinical trials for Peripheral T Cell Lymphoma

Chidamide Plus Azacitidine for the Treatment of Previously Untreated Nodal TFH Cell Lymphoma

Start date: March 2, 2023
Phase: Phase 2
Study type: Interventional

Untreated patients with Nodal T-follicular Helper (TFH) Cell Lymphoma will be treated with chidamide combined with azacitidine for four cycles. For patients with interim evaluation of CR, consolidation therapy with ASCT or another eight cycles with chidamide combined with azacitidine can be obtained. For patients with interim evaluation of PR, another two cycles of chidamide combined with azacitidine will be continued, followed by the second efficacy evaluation, and those who achieve CR receive consolidation therapy with ASCT or another six cycles of chidamide combined with azacitidine. Subsequently, chidamide was given as maintenance therapy for 12 months. Patients with SD or PD withdrew from this study.