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NCT ID: NCT05682547 Not yet recruiting - Clinical trials for Diabetic Eye Problems

Diquafosol vs Hyaluronic Acid for Diabetic Dry Eye

Start date: November 1, 2023
Phase: N/A
Study type: Interventional

Diquafosol ophthalmic solution (DQS) stimulates P2Y2 receptors on the ocular surface, which enhances mucin secretion from goblet cells. Therefore, tear film stability and hydration of the ocular surface can be achieved independent from lacrimal glands function. While it has been observed that 0.1 percent hyaluronate (HA) in artificial tears promotes corneal re-epithelium and improves corneal healing.This prospective, open label pilot study will include 60 eyes of 30 diabetic patients diagnosed with DED and will be randomly assigned to either DQS (n=30 eyes) or ATD group (n=30 eyes). Participants in the DQS group will receive 3% Diquafosol ophthalmic solution, while HA group will receive 0.1% Sodium hyaluronate artificial tears. The dosage for both drugs will be one drop, six times per day for 4 weeks. Tear film lipid layer (TFLL), non-invasive breakup time (NITBUT), corneoconjunctival staining score (CS), meibum gland (MG), conjunctival hyperemia (RS score), ocular surface disease index (OSDI) will be assessed and compared at baseline, day-14, and day-28.

NCT ID: NCT05681403 Not yet recruiting - Lymphoma Clinical Trials

Clinical Study of Improved BEAM Conditioning Regimen for ASCT in Lymphoma

Start date: January 15, 2023
Phase: N/A
Study type: Interventional

This is a single arm, open, single-center clinical study. The patients who are diagnosed with lymphoma and intend to undergo ASCT will be enrolled. The aim of this study is to investigate the efficacy and safety of the conditioning regimen using mitoxantrone hydrochloride liposome, BCNU, etoposide and cytarabine for ASCT.

NCT ID: NCT05677672 Not yet recruiting - Clinical trials for Complex Perianal Fistulas

The Purpose of This Study is to Evaluate the Safety and Efficacy of Human TH-SC01 Cell Injection in the Treatment of Complex Perianal Fistula

Start date: December 30, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of human TH-SC01 cell injection for the treatment of complex perianal fistulas

NCT ID: NCT05677178 Not yet recruiting - Clinical trials for Hemophagocytic Lymphohistiocytoses

Response Prediction in EBV-HLH Using Metabonomics Analysis

Start date: January 1, 2023
Phase:
Study type: Observational [Patient Registry]

Hemophagocytic lymphohistiocytosis (HLH) is a rare, poorly recognized and underdiagnosed syndrome of excessive immune activation, which is rapidly fatal. Epstein-Barr virus (EBV) is a common trigger of HLH, particularly in Asian individuals. We aim to analyze metabolomics and cytokine profiles of patients before and after treatment to explore the metabolomic characteristics of EBV-HLH, and search for pathogenic mechanisms and therapeutic targets.

NCT ID: NCT05675202 Not yet recruiting - Clinical trials for Chronic Kidney Diseases

Material Balance Study of TQ-B3525

Start date: January 2023
Phase: Phase 1
Study type: Interventional

A clinical study to investigate the absorption, metabolism and excretion of [14C] TQ-B3525 in Chinese adult male healthy subjects, aiming to quantitatively analyze the total radioactivity in the excreta of male healthy subjects after oral administration of [14C] TQ-B3525, obtain the data of human radioactive excretion rate and main drainage routes, investigate the distribution in whole blood and plasma, the distribution in plasma and the pharmacokinetics of total radioactivity in plasma, and identify the main metabolites, To determine the main biotransformation pathway and obtain the pharmacokinetic parameters of TQ-B3525 and its metabolites in plasma.

NCT ID: NCT05673538 Not yet recruiting - Clinical trials for Advanced Solid Tumor

TT-00973-MS Tablets in Patients With Advanced Solid Tumors

Start date: January 2023
Phase: Phase 1
Study type: Interventional

This study is a multicenter, open-label, phase 1 study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of TT-00973-MS tablets in patients with solid tumors.

NCT ID: NCT05673525 Not yet recruiting - Aortic Stenosis Clinical Trials

A Clinical Trial of the Transcatheter Aortic Valve Implantation System With a Prospective, Multi-Center, One-Arm Approach to Evaluate the Efficacy and Safety in the Treatment of Patients With Severe Aortic Stenosis

Start date: December 30, 2022
Phase: N/A
Study type: Interventional

A Clinical Trial of the Transcatheter Aortic Valve Implantation System with a Prospective, Multi-Center, One-Arm Approach to Evaluate the Efficacy and Safety in the Treatment of Patients with Severe Aortic Stenosis

NCT ID: NCT05672888 Not yet recruiting - COVID-19 Pneumonia Clinical Trials

Efficacy and Safety of Jaktinib in Patients With COVID-19 Pneumonia.

Start date: March 2023
Phase: Phase 2
Study type: Interventional

This was a randomized, double-blind, placebo-controlled parallel study.

NCT ID: NCT05672498 Not yet recruiting - COVID-19 Clinical Trials

Effect of a Traditional Chinese Medicine Formulation on COVID-19 Infection

Start date: January 5, 2023
Phase: N/A
Study type: Interventional

Traditional Chinese medicine (TCM) has been handed down for thousands of years. It has a long history in the treatment of virus infection and has a good effect on the upper respiratory tract infection. In recent years, the project applicant has been conducting research on the anti infection and anti inflammation treatment of traditional Chinese medicine, and has carried out a lot of clinical practice exploration in non-specific inflammation. The purpose of this research is to study the therapeutic effect of a traditional Chinese medicine prescription on COVID-19 infection.

NCT ID: NCT05672420 Not yet recruiting - Anemia Clinical Trials

Umbilical Cord Derived Mesenchymal Stem Cells for Treatment-induced Myelosuppression in Hematologic Malignancies

Start date: January 1, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to explore the safety and efficacy of umbilical cord derived mesenchymal stem cells in treatment-induced myelosuppression in patients with hematologic malignancies.