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NCT ID: NCT03397550 Withdrawn - Clinical trials for Chronic Kidney Diseases

The Relationship Between Salt Restriction and Taste Sensitivity in Patients With Chronic Kidney Disease

Start date: June 18, 2022
Phase:
Study type: Observational

The compliance of salt restriction in patients with CKD may be associated with taste sensitivity.

NCT ID: NCT03392480 Withdrawn - Clinical trials for Postoperative Delirium

Association of Haptoglobin 2-2 With Postoperative Delirium

Start date: December 20, 2017
Phase:
Study type: Observational

Patients with major orthopedic surgery will be recruited. Participants will be monitored for delirium after surgery. Participants' blood will be harvested for the determination of haptoglobin types, levels of oxidative stress and inflammation. Investigators will then analyze the data to see if haptoglobin 2-2 type is associated with an increased postoperative delirium, inflammation and oxidative stress.

NCT ID: NCT03388242 Withdrawn - Clinical trials for Mild Cognitive Impairment

Protein and microRNA Markers for Early Detection of Alzheimer's Disease

Start date: December 7, 2017
Phase:
Study type: Observational

Blood will be harvested from three groups of people, normal control, patients with mild cognitive impairment (MCI) and patients with Alzheimer's disease (AD), 20 people per group. The blood samples will be used to determine the difference in the expression of microRNAs and proteins. Blood samples will be harvested again at 6-month interval from patients. The combination of the microRNAs and proteins that have different expression patterns between normal control and patients with MCI will be constructed in a kit to detect the difference. This kit will be used in another set of the three groups of people to determine its sensitivity and specificity in detecting patients with MCI.

NCT ID: NCT03382249 Withdrawn - Clinical trials for Carotid Atherosclerosis

Sonodynamic Therapy Manipulates Atherosclerosis Regression Trial on Patients With Carotid Atherosclerotic Plaques

SMART-C
Start date: September 20, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

Sonodynamic therapy (SDT) is a new treatment for carotid atherosclerotic plaque. The aim of this study is to assess the safety and efficacy of this technique.

NCT ID: NCT03380689 Withdrawn - Clinical trials for Metastatic Colorectal Cancer

Phase I Study of Biweekly SIRB Regimen for Metastatic Colorectal Cancer

SIRB2
Start date: January 5, 2018
Phase: Phase 1
Study type: Interventional

Phase I Study of biweekly combination therapy with S-1, Irinotecan, and Bevacizumab as 1-line Chemotherapy in Patients With Advanced Colorectal Cancer.

NCT ID: NCT03378063 Withdrawn - Clinical trials for Bronchopulmonary Dysplasia

Stem Cells for Bronchopulmonary Dysplasia

Start date: November 1, 2017
Phase: Early Phase 1
Study type: Interventional

Very preterm infants are at high risk to develop to bronchopulmonary dysplasia (BPD) for the lack of effective measures to prevent or ameliorate this common and serious disorder. BPD remains a major cause of mortality and lifelong morbidity in preterm infants

NCT ID: NCT03377725 Withdrawn - Clinical trials for Myelodysplastic Syndromes

Decitabine and Arsenic Trioxide for Myelodysplastic Syndrome(MDS)

Start date: March 20, 2018
Phase: Phase 3
Study type: Interventional

This is a prospective,controlled and multi-institution trial.The aim is to identify if using decitabine and Arsenic Trioxide(ATO) as the therapy of Myelodysplastic Syndrome(MDS) has better relapse free survival and complete response than using decitabine alone. TP53 mutation is commonly associated with poor cancer patient prognosis yet no mutant p53 (mp53)-targeting regimen was clinically established. Particularly, p53 mutation is associated with extremely poor prognosis in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) patients. Decitabine (DAC) is a FDA approved drug for MDS treatment. In two independent clinical trials reported recently, DNA demethylating drug DAC treatment yielded a surprisingly high rate of complete remission (CR) in mp53-harboring AML/MDS patients (Welch, NEJM, 2016; Chang, BJH, 2017). Notably, all of the mp53-expressing patients in the two clinical studies relapsed quickly. Arsenic trioxide (ATO) is a FDA approved drug for M3-AML treatment. Despite of the observed efficacy in treating non-APL patients, ATO is not yet approved for non-APL cancer treatment. ATO plays key role in regulating both wild-type p53 (wtp53) and mp53. Our published and unpublished data suggest ATO potentially hijacks nuclear iASPP-mediated STRaND pathway via exposing iASPP's RaDAR nuclear import code (Lu, Cancer Cell, 2013; Lu, Cell, 2014; Lu, Nat Rev Mol Cell Biol, 2016; Lu, unpublished). Our unpublished data also suggests a key role of ATO in regulating mp53 (Lu, The 17th International p53 Workshop, 2017). ATO is widely reported to be able to degrade and thus inhibit mp53's oncogenic function (Hamadeh, BBRC, 1999)(Liu, Blood, 2003). ATO suppressed cancer cell growth by targeting mp53 for degradation by Pirh2 degradation pathway (Yang, JBC, 2011; Yan, PLOS one, 2014); Here we explore the potential of combination of DAC and ATO in improving the mp53-harboring AML/MDS patients' relapse free survival (RFS) and the ability to thoroughly eliminate mp53 subclone. Basic researches aiming to explore the mechanisms how mp53 cells responds to DAC and/or ATO treatment and how mp53 cells develop resistance to DAC and/or ATO will be coupled. We designate trials aiming for a better treatment regimen for mp53 patients as 'PANDA-Trials'.

NCT ID: NCT03373123 Withdrawn - Clinical trials for Esophageal Varices in Cirrhosis of the Liver

Radiomics-based Surrogate of Endoscopy (rEndosc) (CHESS1703)

rEndosc
Start date: December 18, 2017
Phase: N/A
Study type: Interventional

Esophageal varices (EVs) resulting from portal hypertension are a prevalent complication of cirrhosis with a high mortality when variceal hemorrhage (VH) occurs. Screening endoscopy for EVs is recommended for all patients with cirrhosis, and prophylactic treatments are proposed for preventing VH, which may be financially onerous. Therefore, noninvasive tools for diagnosing EVs and risk stratifying VH in cirrhotic patients are needed to decrease the number of unnecessary invasive endoscopic examinations of low-risk patients and avoid unneeded prophylactic treatment. This is a prospective, multi-center diagnostic trial conducted at 9 high-volume liver centers in China designed to determine the diagnostic performance of radiomics-based surrogate (rEndosc) (investigational technology) by CT imaging for noninvasive prediction of EVs and risk stratification of VH in patients with hepatitis B virus-related cirrhosis using endoscopic examinations as reference standard.

NCT ID: NCT03353428 Withdrawn - Lung Cancer Clinical Trials

Intervention of Engineered Immune Effector T Cells Against Lung Cancer

Start date: November 15, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the safety of lung cancer specific cytotoxic lymphocytes (LC-CTLs). The secondary objectives are to evaluate the rate of successful LC-CTLs generation in vitro and determine the anti-lung cancer efficacy.

NCT ID: NCT03353181 Withdrawn - Clinical trials for Endoscopic Retrograde Cholangiopancreatography

Application of Endoscopic Scissors Cutting ENBD Tube in the Treatment of Malignant Hilar Biliary Strictures

ENBD
Start date: November 30, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate application value of the endoscopic cutting technique in the treatment of malignant hilar biliary strictures.