Clinical Trials Logo

Filter by:
NCT ID: NCT05108064 Recruiting - Pituitary Neoplasms Clinical Trials

Radiomic and Pathomic Study of Pituitary Adenoma Using Machine Learning

Start date: January 1, 2019
Phase:
Study type: Observational

Refractory pituitary adenoma is characterized by invasive tumor growth, continuous growth and/or hormone hypersecretion in spite of standardized multi-modal treatment such as surgeries, medications or radiations. Quality of life or even lives are threatened by these tumors. According to the 2017 World Health Organization's new classification guideline of pituitary adenoma, patients have to suffer from symptoms or complications caused by these tumors, to bear a heavy financial burden, and to accept additional therapeutic side effects when the diagnosis of "refractory pituitary adenoma" is made. If refractory pituitary adenoma could be predicted at early stage, these patients would be able to have a more frequent clinical follow-up, receive multiple effective treatment as early as possible, or even be enrolled in clinical trials of investigational medications, so as to prevent or delay the recurrence or persistent of the tumor growth. Therefore, the unmet clinical need falls into an early prediction system for refractory pituitary adenomas, which could provide accurate guidance for subsequent treatment in the early stage. The investigators have constructed a pituitary adenoma database including clinical data, radiological images, pathological images and genetic information. The investigators are proposing a study using machine learning to extract features from these multi-dimensional, multi-omics data, which could be further used to train a prediction model for the risk of refractory pituitary adenoma. The proposed model would also be validated in another prospectively collected database. The established model would be able to identify potential medication targets and provide guidance for personalized therapy of refractory pituitary adenoma.

NCT ID: NCT05107999 Recruiting - Dyspepsia Clinical Trials

Stigma and Efficacy of Zhizhu Kuanzhong Capsules

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

Antidepressants are effective in patients with functional dyspepsia (FD), however, the stigma related with FD and antidepressants could affect treatment adherence and efficacy. Zhi Zhu Kuan Zhong capsules (ZZKZ), a traditional Chinese medicine fomula, showed therapeutic potential for FD. The study was designed to investigate whether ZZKZ could alleviate stigma in FD and obtain identical effects in patients with refractory FD.

NCT ID: NCT05107011 Recruiting - Clinical trials for Advanced Solid Tumor

Phase I/II Clinical Trial of LBL-015 for Injection

Start date: November 5, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

A phase I/II clinical study evaluating LBL-015 in the treatment of subjects with advanced solid tumors

NCT ID: NCT05106972 Recruiting - Liver Cirrhosis Clinical Trials

Umbilical Cord Mesenchymal Stem Cell Transplantation for Decompensated Hepatitis B Cirrhosis

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

This study aims to evaluate the safety and clinical efficacy of umbilical cord mesenchymal stem cell transplantation for decompensated hepatitis B cirrhosis.

NCT ID: NCT05106946 Recruiting - B-cell Malignancy Clinical Trials

Safety and Clinical Activity of ThisCART22 in Patients With r/r Non-Hodgkin's B Cell Lymphoma

Start date: October 25, 2021
Phase: Phase 1
Study type: Interventional

A single arm, open-label, dose-escalation study to evaluate the safety and clinical activity of ThisCART22 (Allogeneic CAR-T targeting CD22) in patients with relapsed and/or refractory non-Hodgkin's B cell lymphoma (r/r B-NHL).

NCT ID: NCT05106907 Recruiting - B-cell Malignancy Clinical Trials

Safety and Clinical Activity of ThisCART19 in Patients With r/r Non-Hodgkin's B Cell Lymphoma

Start date: October 25, 2021
Phase: Phase 1
Study type: Interventional

A single arm, open-label, dose-escalation study to evaluate the safety and clinical activity of ThisCART19 (Allogeneic CAR-T targeting CD19) in patients with relapsed and/or refractory non-Hodgkin's B cell lymphoma (r/r B-NHL).

NCT ID: NCT05106777 Recruiting - Sarcoma Clinical Trials

Surufatinib in Patients With Osteosarcoma and Soft Tissue Sarcoma

Start date: December 10, 2021
Phase: Phase 2
Study type: Interventional

The purpose is to evaluate the effectiveness and safety of Surufatinib in patients with osteosarcoma and soft tissue sarcoma after Standard chemotherapy therapy.

NCT ID: NCT05106699 Recruiting - Prostate Cancer Clinical Trials

Carbon Ion Followed by Proton Radiotherapy for Prostate Cancer With Pelvic Lymph Nodes Metastases

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

The present of clinically pelvic lymph node positive (cN1) represent one of the most important prognostic factors for recurrence and cancer-specific mortality of prostate cancer patients. Approximately 12% of prostate cancer patients present with cN1 disease at the time of diagnosis. Furthermore, with the advent of more sensitive advance diagnostic imaging techniques, such as PSMA PET/CT, the likelihood that pelvic nodes will be found earlier and more frequently. Unfortunately, The optimal treatment for patients with cN1 still remains unclear. Androgen deprivation therapy (ADT) is the cornerstone of prostate cancer with pelvic lymph node metastasis. Some retrospective and database studies have shown that addition of local radiotherapy (RT) to ADT improve the treatment outcome. The 2022 NCCN guideline recommend RT combined with 2 to 3 years ADT in patients with initially diagnosed cN1 prostate cancer who have a life expectancy greater than 5 years.

NCT ID: NCT05106517 Recruiting - Clinical trials for Denosumab vs Zoledronate

Denosumab vs Zoledronic Acid and Osteoporotic Compression Fracture

Start date: September 8, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

Bone mineral density and function at 1 year after screw fixation with denosumab vs zoledronic acid for osteoporotic vertebral compression fractures: a parallel double-blind randomized controlled clinical trial

NCT ID: NCT05106270 Recruiting - Heart Failure Clinical Trials

The Impact of Atrial Pressure Change Before and After Combined Procedure

Start date: November 10, 2021
Phase:
Study type: Observational [Patient Registry]

One-stop procedure combining catheter ablation (CA) and left atrial appendage closure (LAAC) has been a feasible treatment for patients with atrial fibrillation at high risk of stroke and/or bleeding. Although it could achieve considerable rhythm control and stroke prophylaxis, a number of patients has experienced progressive heart failure after the procedure. Notably, previous studies indicate that both pulmonary vein isolation by CA and LAAC could significantly increase left atrial pressure, while currently no study has investigated left atrial pressure change in patients underwent combined procedure. The investigators hypothesise that combined procedure would significantly increase left atrial pressure and subsequently deteriorate cardiac function. Therefore, the investigators aim to measure the left and right atrial pressure change before and after CA and LAAC in combined procedure, and investigate the influence of the pressure change on clinical outcomes.