Ignite Creation Date:
2024-05-05 @ 11:07 AM
Last Modification Date:
2024-10-26 @ 9:05 AM
Study NCT ID:
NCT00006166
Status:
COMPLETED
Last Update Posted:
2010-01-13
First Post:
2000-08-08
Brief Title:
North American Study for the Treatment of Refractory Ascites NASTRA
Sponsor:
National Institute of Diabetes and Digestive and Kidney Diseases NIDDK
Organization:
National Institute of Diabetes and Digestive and Kidney Diseases NIDDK
Study Overview
Official Title:
The North American Study for the Treatment of Refractory Ascites NASTRA Clinical Trial
Status:
COMPLETED
Status Verified Date:
2010-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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 andor distension andor limitation of activity who have either diuretic-resistant ascites or diuretic-intractable ascites are being studied
Detailed Description:
None
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 1R01DK051523 | NIH | None | httpsreporternihgovquickSearch1R01DK051523 |