Ultrafiltration (Aquapheresis) in Patients With Leukemia and Severe Fluid Overload
NCT01508260 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2013-04-05
Summary
The goal of this clinical research study is to learn about the safety and level of effectiveness of aquapheresis compared to diuretic drugs. Diuretic drugs are designed to help the kidneys to form more urine. They also remove fluids from patients with severe fluid overload who have not responded to diuretics.
Aquapheresis is a procedure that removes excess fluid from the body. Blood containing too much salt and water is withdrawn from the body using catheters (sterile flexible tubes) and passed through a special filter. The filter separates the excess salt and water from the blood. The blood is returned to the patient and the fluid is collected in a bag to be disposed. Aquapherisis may benefit patients by removing excess fluid and salt from the body.
Conditions
Interventions
- PROCEDURE
-
Aquapheresis
Participant connected to aquapheresis pump through an intravenous (IV) catheter placed in forearm. Average treatment is about 24 hours but can extend up to 7 days.
- DRUG
-
Furosemide
20-40 mg by vein every 8 hours as indicated for optimal diuresis to achieve negative fluid balance or 0.5 to 5 mg per hour by continuous infusion.
Sponsors & Collaborators
-
M.D. Anderson Cancer Center
lead OTHER
Principal Investigators
-
Gloria Iliescu, MD · UT MD Anderson Cancer Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-03-31
- Primary Completion
- 2018-03-31
More Related Trials
-
Early Discharge With Subcutaneous Furosemide Versus Standard Care in Acute Heart Failure
NCT07018297 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Preoperative Ascites Drainage Versus Standard Care for Patients With Advanced Ovarian Cancer
NCT02742428 ·Status: SUSPENDED ·Phase: NA
-
The Role of Intravenous Albumin Replacement During Abdominal Paracentesis in Patients With Malignancy Related Ascites
NCT02811406 ·Status: UNKNOWN ·Phase: NA
-
Diuretic Efficacy of Aminophylline and Furosemide Combination vs Furosemide Alone in Critically Ill Adults
NCT05933642 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Restrictive Versus Liberal Rate of Extracorporeal Volume Removal Evaluation in Acute Kidney Injury
NCT05306964 ·Status: TERMINATED ·Phase: NA
-
Peritoneal Dialysis vs Furosemide for Acute Kidney Injury After Cardiopulmonary Bypass
NCT01709227 ·Status: COMPLETED ·Phase: NA
-
Stop Hypernatremia, Use Metolazone, for Aggressive, Controlled, Effective Diuresis
NCT01617798 ·Status: WITHDRAWN ·Phase: NA
-
Exploring Water-free Sodium Storage
NCT06872645 ·Status: RECRUITING ·Phase: NA
-
Hemodynamics and Extravascular Lung Water in Acute Lung Injury
NCT00624650 ·Status: COMPLETED ·Phase: PHASE2
-
Kinetics of Surfactant Proteins, Phosphatidylcholine and Body Water in Intensive Care Unit (ICU)
NCT03371680 ·Status: COMPLETED ·Phase: NA
-
CRT Hydration in the Last Days of Life (Feasibility Study)
NCT02344927 ·Status: COMPLETED ·Phase: NA
-
A Total Balanced Volume Replacement Regimen in Elderly Cardiac Surgery Patients
NCT00576849 ·Status: COMPLETED ·Phase: PHASE4
-
Fluid Mobilization in Hospitalized Patients With Acute Kidney Injury
NCT04522635 ·Status: COMPLETED ·Phase: PHASE4
-
Glucocorticoid Therapy for Acute Respiratory Distress Syndrome
NCT05401812 ·Status: WITHDRAWN ·Phase: PHASE2
-
Perfusion Parameters and Outcome During a Standardized Deresuscitation Strategy with Net Ultrafiltration: a Retrospective Cohort Study.
NCT06899880 ·Status: COMPLETED
-
The Efficacy and Safety of Diluted Oral Phosphate Enema Versus Intravenous Sodium Glycerophosphate in The Treatment of Hypophosphatemia in ICU Patients
NCT06651892 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Volume Optimization Incorporating Negative Pressure Diuresis in Heart Failure (VOID-HF)
NCT04227977 ·Status: COMPLETED ·Phase: NA
-
Study in Intensive Care Patients to Investigate the Clinical Effect of Repetitive Orally Inhaled Doses of AP301 on Alveolar Liquid Clearance in Acute Lung Injury
NCT01627613 ·Status: COMPLETED ·Phase: PHASE2
-
Albumin 4 gr/L vs 8 gr/L in the Prevention of Post-Paracentesis Circulatory Dysfunction
NCT00428506 ·Status: UNKNOWN ·Phase: PHASE2
-
Using Furosemide to Prevent Fluid Overload During Red Blood Cell Transfusion in Neonates
NCT00618852 ·Status: UNKNOWN ·Phase: PHASE3
-
The Furosemide Stress Test, Electrolytes Response and Renal Index in Critically Ill Patients
NCT04215419 ·Status: COMPLETED
-
Hypertonic Saline Therapy in Ambulatory Heart Failure Unit.
NCT04533997 ·Status: COMPLETED ·Phase: PHASE3
-
Controlled Fluid Removal in Critical Ill Patients With Fluid Overload in the Intensive Care Unit.
NCT04180397 ·Status: RECRUITING ·Phase: PHASE4
-
Furosemide Stress Test to Predict Successful Liberation From RRT
NCT05612490 ·Status: COMPLETED
-
Zero Sodium Peritoneal Dialysate Protocol Pilot Study
NCT03801226 ·Status: COMPLETED ·Phase: EARLY_PHASE1