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NCT ID: NCT04758416 Recruiting - Breast Cancer Clinical Trials

Study on the Value of Non-invasive Dual-Pet Information in Subtype of Metastatic Breast Cancer

Start date: December 31, 2020
Phase:
Study type: Observational

Study on the Value of Non-invasive Dual-Pet(18F-FES PET and 68Ga-HER2-Affibody PET) Information in Subtype of Metastatic Breast Cancer

NCT ID: NCT04758195 Recruiting - Clinical trials for Low Anterior Resection Syndrome

Transanal Irrigation to Prevent Major Low Anterior Resection Syndrome

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

Bowel dysfunction after rectal cancer resection comprises a vast array of bowel symptoms and associated quality-of-life impairment, collectively termed as low anterior resection syndrome (LARS). There are 40%-60% patients who suffer from major LARS after sphincter-preserving surgery. No consensus exists for LARS treatment or prevention. Transanal irrigation (TAI) was reported to play a helpful role in the management of major LARS and fecal incontinence. However, the preventive effect and daily accessibility need further confirmation. In this randomized trial, TAI compared with best support treatment, is used in patients who received curative low anterior resection for rectal cancer with diverting stoma, after completion of the stoma reversal. The primary outcome is the occurrence of major LARS after 6 months of the treatment.

NCT ID: NCT04757779 Recruiting - Anlotinib Clinical Trials

A Single-arm, Phase Ⅱ Clinical Trial of Anlotinib Hydrochloride Combined With Irinotecan or Docetaxel for Second Line Treatment of Nonsensitive Relapsed Small-cell Lung Cancer

Start date: December 30, 2019
Phase: Phase 2
Study type: Interventional

Anlotinib hydrochloride is a multi-target antiangiogenic drug. It was recommended by Chinese Society of Clinical Oncology(CSCO) guideline as a third-line treatment for advanced small-cell lung cancer. This study intends to assess the efficacy and safety of anlotinib hydrochloride combined with irinotecan or docetaxel for second line treatment of nonsensitive relapsed small-cell lung cancer.

NCT ID: NCT04757597 Recruiting - Clinical trials for Cerebral Amyloid Angiopathy

Remote Ischemic Conditioning for Cerebral Amyloid Angiopathy-related Intracerebral Hemorrhage

RIC-CAAH
Start date: February 24, 2021
Phase: N/A
Study type: Interventional

Cerebral amyloid angiopathy-related intracerebral (CAAH) hemorrhage is second factor of primary intracerebral hemorrhage. However, no effective prevention and treatment strategies have been established. Remote ischemic conditioning is a neuroprotective strategy. In animal studies,RIC is efficiency in accelerating the absorption of hematoma. Therefore, the investigators plan to carry out this research to evaluate the safety and efficacy of RIC in patients with CAA related ICH.

NCT ID: NCT04757350 Recruiting - Cataract Clinical Trials

Objective Visual Quality Analysis System is Used in Cataract

Start date: February 1, 2021
Phase:
Study type: Observational

The Objective Visual Quality Analysis System (OQAS) is a new inspection technology used to objectively assess the visual quality of the human eye. The investigators use this advanced technology to evaluate and follow up cataract patients before and after surgery, and observe the incidence, severity, and treatment effects of postoperative complications such as postoperative complications, and analyze the severity and artificial The influence of lens type, postoperative time, systemic diseases and other factors on the effect of cataract surgery, in order to discover the key factors that affect the effect of cataract surgery and the management of complications, and provide a useful reference for improving the level of cataract prevention and treatment in China

NCT ID: NCT04757129 Recruiting - Clinical trials for Acute Pulmonary Embolism

Changes of Cardiopulmonary Function After Thrombolysis in Patients With Pulmonary Embolism

CCFATAPE
Start date: January 1, 2020
Phase:
Study type: Observational

The investigators expect to enroll about 80-100 acute pulmonary embolism patients treated with thrombolysis in two hospitals. Dynamic changes of cardiopulmonary function after thrombolysis are detected to evaluate which indicators can quickly reflect the effectiveness of thrombolysis.

NCT ID: NCT04756934 Recruiting - Melanoma Clinical Trials

A Study of HX008 Plus LP002 for the Treatment of Patients With Advanced Melanoma

Start date: August 20, 2020
Phase: Phase 1
Study type: Interventional

The subsequent treatment choices for the patients with advanced melanoma, who have failed the immune checkpoint inhibitor therapy of single agent. Evidences showed that PD-1 and PD-L1 signalling pathways are not redundant. Blocking both of them could produce synergistic effect. HX008 and LP002 are humanized monoclonal antibodies targeting PD-1 on T cells and PD-L1 on tumor cells respectively. In this study, participants with locally advanced or metastatic melanoma who have failed previous anti-PD-1 or PD-L1 will be administrated with HX008 plus LP002. The safety and preliminary efficacy will be evaluated.

NCT ID: NCT04756648 Recruiting - Clinical trials for Advanced Hepatocellular Carcinoma

Phase I Clinical Trial of CT0180 Cells in the Treatment of Hepatocellular Carcinoma

Start date: March 10, 2021
Phase: Phase 1
Study type: Interventional

A Phase I Clinical Study ofCT0180 cells in Patients with Advanced Hepatocellular Carcinoma

NCT ID: NCT04755907 Recruiting - Colorectal Cancer Clinical Trials

3D Bioprinted Models for Predicting Chemotherapy Response in Colorectal Cancer With/Without Liver Metastases

Start date: March 1, 2021
Phase:
Study type: Observational

The therapeutic regimens of adjuvant and neoadjuvant chemotherapy for colorectal cancer (CRC) remain largely relied on clinical experience, and thus preclinical models are needed to guide individualized medicine. The investigators are going to establish 3D bioprinted CRC models and organoids from surgically resected tumor tissues of CRC patients with or without liver metastases. In vitro 3D models and organoids will be treated with the same chemotherapy drugs with the corresponding patients from whom the models are derived. The sensitivity of chemotherapy drugs will be tested in these two types of in vitro models, and the actual response to chemotherapy in patients will be evaluated. The predictive ability of 3D models for chemotherapy sensitivity in CRC patients will be compared with that of the organoids. This observational study will validate the potential value of 3D bioprinted tumor models in predicting the response to chemotherapy in CRC.

NCT ID: NCT04755543 Recruiting - Clinical trials for Digestive System Neoplasms

A Study of LP002 for the Treatment of Patients With Malignant Digestive System Neoplasms

Start date: June 17, 2019
Phase: Phase 1
Study type: Interventional

LP002 is a humanized monoclonal antibody targeting programmed death ligand-1 (PD-L1), which prevents PD-L1 from binding to PD-1 and B7.1 receptors on T cell surface, restores T cell activity, thus enhancing immune response and has potential to treat various types of tumors. In this study, the safety, pharmacokinetics and preliminary efficacy of LP002 for the treatment of malignant digestive system neoplasms will be evaluated.