Clinical Trials Logo

Filter by:
NCT ID: NCT06357806 Recruiting - Chronic Hepatitis B Clinical Trials

The Treatment of PD-1 Antibody Combined With Peg-IFNα in NAs-suppressed CHB Patients

Start date: June 6, 2024
Phase: N/A
Study type: Interventional

This is a prospective, open-labled, randomized controlled study to assess efficacy and safety of treatment with Sintilimab (PD-1 antibody) combined Peg-IFNα-2b in CHB patients on stable NAs treatment.

NCT ID: NCT06357741 Completed - Knee Osteoarthritis Clinical Trials

Clinical Study of Desuzumab in the Treatment of Knee Osteoarthritis

CSODITTOKO
Start date: March 2, 2023
Phase:
Study type: Observational

As an activator of inhibiting nuclear factor kB receptor, denosumab affects osteoclast differentiation and development by inhibiting OPG/RANKL-RANK bone regulatory axis pathway. Therefore, denosumab is widely used in the treatment of bone diseases such as osteoporosis. Osteoporosis is closely related to knee osteoarthritis. RANKL-RANK pathway also plays a key role in the pathogenesis of knee osteoarthritis. Therefore, the investigators propose the hypothesis that denosumab can effectively treat knee osteoarthritis.

NCT ID: NCT06357598 Recruiting - Clinical trials for Non-small-cell Lung Cancer (NSCLC)

Preoperative Neoadjuvant Immunotherapy Combined With Chemotherapy for Stage Ⅲ Unresectable Non-small Cell Lung Cancer

PILOT
Start date: January 18, 2024
Phase: Phase 4
Study type: Interventional

Explorative study, which evaluates the effect of Tislelizumab combined with chemotherapy in neoadjuvant treatment of stage Ⅲ unresectable non-small-cell lung carcinoma.

NCT ID: NCT06357117 Completed - Clinical trials for Perihilar Cholangiocarcinoma

Extent of Intrahepatic Infiltration of Perihilar Cholangiocarcinoma

Start date: April 13, 2018
Phase:
Study type: Observational

The extent of intrahepatic infiltration of perihilar cholangiocarcinoma (PHCC) remains unclear. This research aimed to explore the pattern and extent of intrahepatic infiltration of PHCC to guide surgical treatment and pathological research. This prospective study included 62 participants diagnosed with PHCC who underwent major hepatectomy. A whole-mount digital liver pathology system (WDLPS) for hepatectomy specimens greater than 10 × 10 cm was used to panoramically assess the intrahepatic infiltration extent of PHCC.

NCT ID: NCT06357104 Completed - Clinical trials for COVID-19 Vaccine Adverse Reaction

Detoxification From the Lipid Tract

Start date: February 26, 2024
Phase: Phase 4
Study type: Interventional

Apart from electroencephalogram biofeedback and electrical brain stimulation adopted for maintenance treatment, the study utilizes ultra-low frequency transcranial magnetic stimulation (ULF-TMS) for initial γ-aminobutyric acid (GABA) stimulation. The cocktail therapy starts after the primary efficacy endpoint, and concomitant therapy is adopted throughout the study.

NCT ID: NCT06357026 Not yet recruiting - Clinical trials for Coronary Artery Disease

Phitys I™ Percutaneous Left Ventricular Assist System Study

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

The primary purpose of this clinical trial is to evaluate the safety and efficacy of the percutaneous left ventricular assist system versus intra-aortic balloon pump (IABP) for Circulatory Support during High-risk PCI.

NCT ID: NCT06356701 Recruiting - Clinical trials for Long-Term Effects Secondary to Cancer Therapy

Tumor Nutritional Therapy in the First-line Treatment of Stage IV NSCLC

Start date: April 15, 2024
Phase: Phase 1
Study type: Interventional

A Single-center, Randomized, Controlled Clinical Study Comparing the Efficacy and Safety of Tumor Nutritional Therapy Combined With Immune Checkpoint Inhibitors and Chemotherapy in the First-line Treatment of Stage IV NSCLC Without Driver Gene Mutations

NCT ID: NCT06356662 Recruiting - Parkinson Disease Clinical Trials

Tenofovir Disoproxil Fumarate in the Treatment of Parkinson's Disease

Start date: January 23, 2024
Phase: Phase 1
Study type: Interventional

To evaluate the efficacy and safety of tenofovir disoproxil fumarate in the treatment of Parkinson's disease. The changes of motor symptoms and the occurrence of adverse reactions in early Parkinson's disease patients who took tenofovir disoproxil fumarate and did not take Tenofovir disoproxil fumarate at different time points were compared.

NCT ID: NCT06356597 Recruiting - Colorectal Cancer Clinical Trials

Tislelizumab With Fruquintinib, Metronidazole, in Mismatch Repair-proficient or Microsatellite Stability, Advanced Colorectal Cancer: a Multicenter, Single Arm, Clinical Trial

Start date: April 1, 2024
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate the efficacy and safety of Tislelizumab with Fruquintinib, Metronidazole treatment in MSS/MSI-L advanced colorectal cancer patients with high abundance of Fusobacterium nucleatum in a single arm Phase II clinical.

NCT ID: NCT06356584 Recruiting - Colorectal Cancer Clinical Trials

Sintilimab Combined With Fruquintinib/Regorafenib ± Radiotherapy for Third-line Treatment of Advanced Metastatic Colorectal Cancer

Start date: April 1, 2024
Phase: Phase 2
Study type: Interventional

Colorectal cancer (CRC) is a significant cause of morbidity and mortality worldwide. Its early clinical manifestations are often subtle, leading to late-stage diagnosis in about 30% of cases with distant metastases. Liver metastases are widespread and associated with poor prognosis, especially in terms of response to immunotherapy. Despite advancements in first- and second-line treatments, third-line therapies for advanced CRC remain limited, emphasizing the need for novel strategies. This prospective study evaluates the efficacy of combined therapy involving Sintilimab, Fruquintinib/Regorafenib, and radiotherapy in advanced CRC. The study cohort comprises patients with non-liver metastatic advanced CRC and those with liver metastases, each receiving tailored treatment protocols. The primary objectives are to assess progression-free survival (PFS), overall survival (OS), and treatment response rates. Subgroup analyses will focus on liver metastases to delineate their impact on treatment outcomes. The rationale for this study stems from the intricate interplay between immunotherapy, targeted therapy, and radiotherapy in CRC management. Previous data suggest a negative correlation between liver metastases and immunotherapy efficacy, necessitating a comprehensive approach integrating multiple treatment modalities. Radiotherapy, particularly stereotactic body radiation therapy (SBRT), has shown promise in controlling liver tumors and modulating the tumor microenvironment, potentially enhancing immunotherapy responses. This study aims to provide valuable insights into optimizing third-line and subsequent therapies for advanced CRC by elucidating the efficacy and safety of this combined treatment approach. The findings may pave the way for personalized treatment strategies tailored to individual patient characteristics, ultimately improving clinical outcomes in this challenging disease setting.