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NCT ID: NCT04657328 Recruiting - Ultrasound Clinical Trials

Prospective Multicenter Study on Clinical Application of Sonazoid in Breast Tumor

Start date: August 15, 2020
Phase:
Study type: Observational [Patient Registry]

Sonazoid as a new generation of ultrasound contrast agent.This study based on the features of Sonazoid specific angiography and high mechanical index,the role of Sonazoid in the differential diagnosis of breast benign and malignant tumors was explored.

NCT ID: NCT04657133 Recruiting - Clinical trials for Intracerebral Hemorrhage

Remote Ischemic Conditioning for the Treatment of Intracerebral Hemorrhage

RICH-2
Start date: April 22, 2021
Phase: Phase 3
Study type: Interventional

Intracerebral hemorrhage (ICH) results from the rupture of small vessels damaged by chronic hypertension, amyloid angiopathy or other disease. Currently, ICH has been a devastating type of stroke that lacking effective therapy. Remote ischemic conditioning (RIC), a systematically protective strategy, has been found to have neuroprotective effects by in patients with ischemic stroke. In addition, animal studies show that RIC is safe in ICH model and it could accelerate the absorption of hematoma. In a previous clinical study (RICH-1), RIC have been found to be safe and well-tolerated in patients with ICH. Therefore, the investigators plan to undertake this study to further evaluate the safety and efficacy of RIC in patients with ICH. The investigators hypothesize that treatment with RIC will accelerate the absorption of hematoma and improve patients' functional outcomes. Results of this study can potentially bring into account new means to improve the outcomes of ICH patients.

NCT ID: NCT04656119 Recruiting - Cancer Clinical Trials

Discovery of Biomarkers Related to the Efficacy and Adverse Reactions of Immune Checkpoint Inhibitors Based on Metabolism-genomics

Start date: November 3, 2020
Phase:
Study type: Observational

Immune checkpoint inhibitors (ICIs) are an important breakthrough in cancer therapy and have been increasingly used.However, ICIs can cause a unique spectrum of side effects termed immune-related adverse events (irAEs),which can affect any organ systems and in some cases are fulminant or even fatal.In clinical practice, irAEs and clinical efficacy maybe various for patients with same standard treatment, and some studies have shown that gene and metabolic differences in cancer patients may be an important factor. In this project, peripheral blood samples from cancer patients will be collected prospectively at baseline, and at regular intervals (2 cycles, about 6 weeks) for about 30 weeks, then these blood samples will be analyzed using the technique of genomics, metabonomics. The investigators aim to find biomarkers associated with irAE or clinical efficacy. When the sample size and data is big enough, the investigators plan to establish a prediction model using machine learning to access the safety and efficacy of ICIs for cancer patients. Our study have important clinical implications in the prediction and early management of severe, potentially life-threatening immune-related toxicity.

NCT ID: NCT04655677 Recruiting - Clinical trials for Non-Hodgkin's B-cell Lymphoma

A Study of EXP039 Treatment in Subjects With r/r NHL Subjects

Start date: August 25, 2020
Phase: Phase 1
Study type: Interventional

This is a single-center, non-randomized study to evaluate the safety and efficacy of EXP039 in relapsed and/or refractory NHL patients.

NCT ID: NCT04653480 Recruiting - Colorectal Cancer Clinical Trials

Surufatinib, Toripalimab and Chemotherapy in Second-line MT and MSS CRC

Start date: February 1, 2021
Phase: Phase 2
Study type: Interventional

To determine the efficacy and safety of surufatinib, toripalimab and chemotherapy in second-line RAS/BRAF mutant and MSS colorectal cancer

NCT ID: NCT04653337 Recruiting - Depression Clinical Trials

Neuroimaging Guided and Robot-assisted rTMS for Suicidal Ideation of Depression

Start date: September 28, 2020
Phase: Phase 2
Study type: Interventional

There is relatively insufficient evidence on whether rTMS can improve suicidal ideation in depressive patients. And existing studies have been inconsistent in the treatment of depressive suicidal thoughts. The possible reason is inaccurate stimuli localization. Improving the accuracy of rTMS stimulus positioning may further improve the intervention effect of suicidal ideation. This study will introduce an automated TMS system with robot control and optical sensor combined with neuronavigation softwarea. By using the robot based on neuronavigation system, the rTMS coil can be accurately positioned over any preselected brain region. An infrared optical measurement device is also used in order to detect and compensate for head movements of the patient. The purpose of this randomized double-blind and sham-controlled study is to test the efficacy and safety of robot-assisted rTMS based on neuronavigation in the treatment of depressive suicidal ideation.

NCT ID: NCT04652492 Recruiting - Clinical trials for Hepatocellular Carcinoma

Tislelizumab in Combination With TACE in Advanced Hepatocellular Carcinoma

Start date: October 27, 2020
Phase: Phase 2
Study type: Interventional

A multicentric, open-label, single-arm prospective study to assess the efficacy and safety of tislelizumab combined with TACE as first-line treatment in patients with unresectable BCLC stage C HCC.

NCT ID: NCT04652440 Recruiting - Clinical trials for Hepatocellular Carcinoma

Ablation Combined With PD-1 in HCC: Phase II Study

Start date: December 15, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase 2, single arm, single center study designed to evaluate the safety and tolerability of radiofrequency or microwave ablation combined with PD-1 monoclonal antibody in patients with hepatocellular carcinoma(HCC), with the secondary study objective to preliminarily evaluate the efficacy of radiofrequency or microwave ablation combined with PD-1 monoclonal antibody in patients with HCC and the exploratory study objective to evaluate the effect of ablation combined with PD-1 monoclonal antibody on immune function and hepatitis virus infection status in patients with HCC. This study will be divided into two stages, and the first stage is to enroll 6 patients for dose-limited toxicity (DLT) observation. If DLT appeared in < 2 patients, the second stage was entered and the other 24 patients were further enrolled.

NCT ID: NCT04652427 Recruiting - Clinical trials for Sedation Complication

Application of Dexmedetomidine Hydrochloride Injection in Anesthesia for Patients Without Tracheal Intubation

Start date: August 20, 2020
Phase: N/A
Study type: Interventional

With 0.9% sodium chloride injection as a placebo control, to evaluate the effectiveness and safety of dexmedetomidine hydrochloride injection for sedation in patients with non-tracheal intubation

NCT ID: NCT04651998 Recruiting - Clinical trials for Carotid Artery Stenosis

Effect of Carotid Artery Stent on Evoked Cerebral Blood Oxygenation and Neurocognitive Functioning

Start date: May 1, 2021
Phase:
Study type: Observational [Patient Registry]

Cerebral hemodynamic compromise from internal carotid artery stenosis may be a cause of vascular cognitive impairment that is amenable to treatment by revascularization. The effect of carotid artery stent on evoked cerebral blood oxygenation and neurocognitive functioning will be evaluated by functional near-infrared spectroscopy. Carotid artery stent could benefit cerebral blood oxygenation after stent and improving neurocognitive functioning after 6 months.