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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT02812186 Completed - Prostate Cancer Clinical Trials

Deep Versus Moderate Neuromuscular Blockade During Laparoscopic Surgery

Start date: December 27, 2016
Phase: Phase 4
Study type: Interventional

This is a two period cross-over study randomizing patients undergoing laparoscopic surgery into 2 different groups: group 1 in which patients receive "deep neuromuscular blockade" in the beginning portion of their laparoscopic surgery followed by a period of "moderate blockade" and, group 2 in which patients receive "moderate neuromuscular blockade" in the beginning portion of their laparoscopic surgery followed by a period of "deep blockade". The deep neuromuscular block is defined as post tetanic count of 1 to 2 and the moderate neuromuscular block is defined as 1-2 twitches. In all patients, sugammadex is used to reverse the block at the end of surgery in order to obtain optimal extubating conditions.

NCT ID: NCT02809183 Completed - Acidosis Clinical Trials

Evaluation of TRC101 in Subjects With Chronic Kidney Disease and Metabolic Acidosis

Start date: March 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This was a double-blind, placebo-controlled, parallel-design, 6-arm, fixed dose study. The study enrolled 135 adult male and female subjects with Stage 3 or 4 chronic kidney disease and low serum bicarbonate levels. The study was conducted in two parts. In Part 1 study drug dosing (TRC101 or placebo) continued for 14 days twice daily (BID). In Part 2 study drug dosing (TRC101 or placebo) continued for 14 days once daily (QD). The maximum study duration per subject was anticipated to be up to 42 days.

NCT ID: NCT02808572 Recruiting - Clinical trials for Chronic Kidney Disease

New Biomarkers of Bone Mineral Metabolism as Cardiovascular Risk Factors in Chronic Kidney Disease Patients

Start date: March 12, 2013
Phase: N/A
Study type: Interventional

To evaluate the relationships between bone mineral metabolism markers (osteoprotegerin, fibroblast growth factor 23) at inclusion and the occurence of cardiovascular events during a 7 year follow-up.

NCT ID: NCT02808351 Completed - Diabetes Mellitus Clinical Trials

Berberine Prevent Contrast-induced Nephropathy in Patients With Diabetes

Start date: July 2016
Phase: Phase 4
Study type: Interventional

The number of cardiac angiography and percutaneous coronary interventions (PCI) has increased steadily in recent years. This has resulted in the increasing incidence of contrast-induced nephropathy (CIN). Major risk factors for CIN include older age, diabetes mellitus (DM), chronic kidney disease(CKD), the concurrent use of nephrotoxic drugs, hemodynamic instability, etc. Importantly, DM appears to act as a risk multiplier, meaning that in a patient with CKD it amplifies the risk of CIAKI. The aim of this multicenter prospective, randomized, controlled study is to evaluate whether berberine treatment during and after the perioperative period would reduce the risk of CIN in a high-risk population of patients with both DM and CKD undergoing coronary angiography or noncoronary angiography, and the influence of such potential benefit on short-term outcome.

NCT ID: NCT02808052 Terminated - Healthy Subjects Clinical Trials

Evaluate Safety and Pharmacokinetics of Minocin (Minocycline) for Injection in Subjects With Renal Insufficiency

Start date: May 29, 2017
Phase: Phase 1
Study type: Interventional

This is a Phase 1, open-label, single-dose study of the safety, tolerability, and pharmacokinetics of Minocin® (minocycline) for injection in subjects with renal insufficiency.

NCT ID: NCT02806505 Completed - Clinical trials for Hepatitis C, Chronic

HELPS Study - A Study of Peginterferon Alfa-2a (Pegasys) in Patients With Chronic Hepatitis C (CHC) and End-Stage Renal Disease (ESRD)

Start date: June 2004
Phase: Phase 3
Study type: Interventional

This study evaluated the safety and efficacy of peginterferon alfa-2a monotherapy in participants with Chronic Hepatitis C (CHC) who have End-Stage Renal Disease (ESRD) and were undergoing hemodialysis.

NCT ID: NCT02806362 Withdrawn - Clinical trials for Chronic Hepatitis C Virus

Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b Chronic Hepatitis C Virus (HCV) Infection With End Stage Renal Disease (ESRD) on Hemodialysis (HD)

GIFT-R
Start date: September 2016
Phase: Phase 3
Study type: Interventional

The purpose of this multicenter, single-arm, combination-drug study, which includes 12 weeks of treatment and 24 weeks of follow-up, is to evaluate the safety, efficacy and pharmacokinetics of ombitasvir/paritaprevir/ritonavir in Japanese adults infected with HCV GT1b, who are treatment-naïve or treatment-experienced to an IFN-based regimen and who have ESRD on HD.

NCT ID: NCT02806089 Completed - Clinical trials for Chronic Kidney Disease

Determinants of Muscle Strength in Chronic Kidney Disease

Start date: January 4, 2016
Phase: N/A
Study type: Interventional

Aim of this study is to determine in chronic kidney disease patients: - the involvement of malnutrition inflammation and atherogenesis syndrome (increase in C reactive protein and decrease in serum albumin) on voluntary muscle strength impairment - the relationship between voluntary muscle strength and muscle mass - the relationship between voluntary muscle strength and lean body mass - the correlation between voluntary muscle strength and physical activity

NCT ID: NCT02805348 Completed - Clinical trials for Chronic Kidney Disease

Post-marketing Surveillance of Bixalomer in Patients With Pre-dialysis Chronic Kidney Disease

Start date: June 1, 2016
Phase:
Study type: Observational

The objective of this study is to assess the long-term safety and efficacy of bixalomer under post-marketed setting.

NCT ID: NCT02805244 Completed - Clinical trials for Anemia of Chronic Kidney Disease

Mass Balance Study of JTZ-951 in Subjects With End-stage Renal Disease on Hemodialysis

Start date: June 2016
Phase: Phase 1
Study type: Interventional

A mass balance study to determine the routes and rates of elimination of radioactivity, to determine total radioactivity in plasma and whole blood over time and compare levels to JTZ-951 and drug-derived entities in plasma and to determine pharmacokinetic (PK) parameters of JTZ-951 and its metabolite(s).