Clinical Trials Logo

Ascites clinical trials

View clinical trials related to Ascites.

Filter by:

NCT ID: NCT00240045 Completed - Refractory Ascites Clinical Trials

The Use of Drugs to Improve Kidney Function in Patients With Liver and Kidney Dysfunction

Start date: October 2005
Phase: Phase 2/Phase 3
Study type: Interventional

We will address the hypothesis that refractory ascites and Type 2 hepatorenal syndrome are mediated in part by diminished circulatory volume and that treatment with midodrine, octreotide and albumin can improve renal and patient outcomes by restoring effective circulating volume and systemic perfusion. Our primary objective is to assess change in creatinine clearance using inulin. We will enroll 15 patients with Type 2 hepatorenal syndrome or refractory ascites once inclusion and exclusion criteria are satisfied. They will be treated for 1 month with octreotide LAR, albumin and midodrine. Renal, serum and neurohormonal parameters will be measured before, during, and after initiation of drug and compared.

NCT ID: NCT00239096 Recruiting - Ascites Clinical Trials

Prevention of Decompensation in Liver Cirrhosis

Start date: September 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether losartan, an angiotensin II blocker prevents the sodium retention in patients with liver cirrhosis and by that reduces the fluid retention. Moreover is the purpose to asses whether losartan is antifibrotic.

NCT ID: NCT00182754 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Octreotide in Treating Patients With Cancer-Related Malignant Ascites

Start date: October 2005
Phase: Phase 3
Study type: Interventional

RATIONALE: Octreotide may be an effective treatment for malignant ascites. It is not yet known whether octreotide is more effective than a placebo in treating malignant ascites. PURPOSE: This randomized phase III trial is studying octreotide to see how well it works compared to placebo in treating patients with cancer-related malignant ascites.

NCT ID: NCT00115947 Completed - Cirrhosis Clinical Trials

Renal and Cardiovascular Effects of Terlipressin in Patients With Cirrhosis and Ascites

Start date: December 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate the effect of terlipressin on myocardial perfusion and renal function. Hypothesis: Significant improvement of renal function reflected by: glomerular filtration rate (GFR), renal blood flow (RBF), excretion of salt and metabolites in the urine and related hormones and peptides in the blood. No effect on the systolic function of the heart.

NCT ID: NCT00108355 Completed - Cirrhosis Clinical Trials

Vasoconstrictors as Alternatives to Albumin After Large-Volume Paracentesis (LVP) in Cirrhosis

Start date: December 2003
Phase: Phase 4
Study type: Interventional

This clinical trial compares a combination of two drugs that constrict blood vessels (Octreotide LAR and Midodrine) to albumin after large volume paracentesis. Subjects have cirrhosis and ascites.

NCT ID: NCT00006166 Completed - Liver Cirrhosis Clinical Trials

North American Study for the Treatment of Refractory Ascites (NASTRA)

Start date: March 1997
Phase: Phase 3
Study type: Interventional

The NASTRA Clinical Trial is a multi-center, randomized, controlled clinical trial designed to determine if treatment with transjugular intrahepatic portasystemic shunts (TIPS) is superior to high volume paracentesis (total paracentesis, TP) for the treatment of refractory ascites due to cirrhosis. Only patients with clinically tense symptomatic ascites (shortness of breath, umbilical hernia, abdominal pain and/or distension, and/or limitation of activity) who have either diuretic-resistant ascites or diuretic-intractable ascites are being studied.

NCT ID: NCT00005906 Completed - Ascites Clinical Trials

Treatment With Octreotide in Patients With Lymphangioleiomyomatosis

Start date: June 2000
Phase: Phase 2
Study type: Interventional

Lymphangioleiomyomatosis (LAM), a disease primarily of women of child-bearing age, is characterized by cystic lung disease and abdominal tumors (e.g., angiomyolipomas). Within the LAM patient population is a subset of patients who develop chylous effusions and lymphangioleiomyomas. Treatment of many of these symptoms has been ineffective. Previous studies with somatostatin and octreotide in other clinical settings have shown reduction in chylous effusions. This study assesses the effectiveness of octreotide in symptomatic patients with LAM, lymphangioleiomyomas and/or chylous effusions/ascites, peripheral lymphedema and chyluria.