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NCT ID: NCT05025215 Recruiting - Inhalation Clinical Trials

The Effect of Precise Aerosol Inhalation Nursing on Sputum Excretion in Elderly Patients With Lung Surgery

Start date: May 8, 2021
Phase: N/A
Study type: Interventional

Comparing the effects of different kinds of aerosol inhalation nursing programs on effective sputum excretion in elderly patients with lung surgery.

NCT ID: NCT05025046 Recruiting - Thyroid Cancer Clinical Trials

NGS-based Thyroscan Genomic Classifier in the Diagnosis of Thyroid Nodules

Start date: September 2021
Phase:
Study type: Observational

The purpose of this study is to evaluate the accuracy of Thyroscan in the differential diagnosis of benign and malignant thyroid nodules with suspecious ultrasound features

NCT ID: NCT05024812 Recruiting - Clinical trials for Metastatic Gastric Cancer

Fruquintinib Combined With Toripalimab and SOX Regimen in the First-line Treatment of Advanced Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma

Start date: June 1, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

This is a prospective, open-label, multicenter, single arm phase Ⅰb/Ⅱ clinical study aims to explore the efficacy and safety of fruquintinib combined with toripalimab and SOX regimen in the first-line treatment of unresectable advanced metastatic gastric or gastroesophageal junction adenocarcinoma.

NCT ID: NCT05024539 Recruiting - Clinical trials for Hepatocellular Carcinoma

Real-World Effectiveness of Regorafenib in the Treatment of Patients With Hepatocellular Carcinoma

Start date: June 20, 2021
Phase:
Study type: Observational

Real-World Effectiveness of Regorafenib in the Treatment of Patients With Hepatocellular Carcinoma

NCT ID: NCT05024526 Recruiting - Clinical trials for Acute Ischemic Stroke

Protective Effects of Edaravone Dexborneol

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The patients of acute ischemic stroke were divided into two groups, edaravone dexborneol treatment group and edaravone treatment group. The purpose of this study was to observe the changes of imaging and the improvement of NIHSS and mRS in different groups.

NCT ID: NCT05024513 Recruiting - Clinical trials for Perihilar Cholangiocarcinoma

Biliary Drainage Plus HAIC in Locally Advanced pCCA

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

Biliary drainage and stent placement remains to be the main palliative treatment choice for advanced perihiliar cholangiocarcinoma (pCCA), and the life expectancy is only 4-6 months. Previous single center prospective phase 2 trial showed that hepatic arterial infusion chemotherapy (HAIC) with oxaliplatin and 5-fluorouracil was an encouraging treatment choice for advanced pCCA due to its high tumor control, survival benefit, and low toxicity. Thus, the multicenter prospective controlled trial was designed to explore and confirm the survival benefit of biliary drainage plus hepatic arterial infusion chemotherapy with oxaliplatin and 5-fluorouracil compared with biliary drainage plus best support care treatment in locally advanced pCCA patients.

NCT ID: NCT05024357 Recruiting - Clinical trials for Precursor Cell Lymphoblastic Leukemia-Lymphoma

A Study of TKI Maintenance Therapy Following Allo-HSCT in Newly Diagnosed Ph+ Adult ALL

Start date: September 6, 2021
Phase: N/A
Study type: Interventional

This project is a key clinical research project approved by the Clinical Research Center of the First Affiliated Hospital of Xi 'an Jiaotong University.Tyrosine kinase inhibitors (TKI) combined with chemotherapy and subsequent allogeneic hematopoietic stem cell transplantation (allo-HSCT) are routinely used in patients with philadelpha-positive lymphoblastic leukemia (Ph+ALL). However, TKI maintenance therapy post-HSCT remains controversial. In this study, Ph+ALL patients are enrolled and given dasatinib combined with chemotherapy followed by allo-HSCT. Then patients in the group A continuing to use dasatinib for 1 year is compared with those in the group B receiving dasatinib for 6 months after HSCT. The measurable residual disease (MRD), complete remission (CR), overall survival (OS), disease free survival (DFS), non-relapse mortality (NRM) and the incidence of graft versus host disease (GVHD) will be observed to determine the optimal duration of TKI maintenance therapy post-HSCT.

NCT ID: NCT05024305 Recruiting - Clinical trials for Advanced Malignancies

Safety, Tolerability, PK, PD, Immunogenicity and Efficacy of TWP-102 in Patients With Advanced Malignancies.

Start date: March 8, 2022
Phase: Phase 1
Study type: Interventional

This is a multi-center, phase I, open clinical study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity and efficacy of TWP-102 injection in patients with advanced malignancies. This study consists of two parts, including a dose escalation study and a dose expansion study. The criteria for dose escalation will be based on the Bayesian optimal interval (BOIN) design with sequentially enrolled cohorts.

NCT ID: NCT05024292 Recruiting - Ischemic Stroke Clinical Trials

Oriental Research AlliaNce of Acute Ischemic Stroke Given Endovascular Treatment

ORANGE
Start date: January 1, 2022
Phase:
Study type: Observational

To determine the safety and efficacy of in situ ischemic postconditioning immediately after successful reperfusion in AIS patients underwnet EVT.

NCT ID: NCT05024266 Recruiting - Immunotherapy Clinical Trials

Tislelizumab Combined With Chemotherapy as Neoadjuvant Therapy for Stage IIIA-IIIB (N2) Lung Squamous Cell Carcinoma

TACT
Start date: August 1, 2021
Phase: Phase 2
Study type: Interventional

Tislelizumab combined with chemotherapy has shown good efficacy and safety in clinical studies of lung adenocarcinoma (RATIONALE 304) and lung squamous cell carcinoma (RATIONALE 307), thus has been approved as the first-line therapy for advanced non-small cell lung cancer (NSCLC) in China. However, there is no data in the field of neoadjuvant therapy for NSCLC. This single-arm, single-center phase II clinical study is designed to evaluate the efficacy, safety and major pathological response (MPR) of Tislelizumab combined with chemotherapy as neoadjuvant therapy in patients with stage IIIA-IIIB (N2) lung squamous cell carcinoma. Biomarkers correlated with efficacy outcomes will also be explored.