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NCT00108355 · ClinicalTrials.gov registry record · Phase 4

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

A Phase 4 study of Cirrhosis and Ascites, sponsored by US Department of Veterans Affairs.

Completed
Registry status
Phase 4
Development phase
29
Enrollment target
1
Study location

NCT00108355: Completed Phase 4 study of Cirrhosis and Ascites, sponsored by US Department of Veterans Affairs.

NCT00108355 is a Phase 4 study of Cirrhosis and Ascites that has completed, run by US Department of Veterans Affairs. The registered enrollment target is 29 participants, below the 90,408-participant average among 53 other Cirrhosis trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00108355, a Phase 4 study of Cirrhosis and Ascites, has completed, sponsored by US Department of Veterans Affairs.

COMPLETED
Registry status
Phase 4
Development phase
29 participants
Enrollment target
1
Study location

Study Summary

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.

Primary Outcome

Comparison between Albumin (Control group) and Vasoconstrictor (Treatment group)

Conditions Studied

Interventions

  • DRUG Midodrine
  • DRUG Octreotide LAR
  • DRUG Albumin
  • DRUG Intravenous Saline Infusion (Albumin placebo)
  • DRUG Oral tablet (Midodrine placebo)

Study Locations (1)

Connecticut

  • VA Connecticut Health Care System (West Haven) - West Haven

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2003-12
Est. Completion 2012-08
Phase Phase 4
US Department of Veterans Affairs

632 total trials

What the finished NCT00108355 record still lists

NCT00108355 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 90,408-participant average among 53 other Cirrhosis trials with a reported enrollment target (100% lower).

The record links to 2 conditions, with Cirrhosis appearing as the primary indexed condition, and to 5 interventions - of which Midodrine is the first listed.

NCT00108355 reports a single indexed study location in Connecticut.

Frequently Asked Questions

What is clinical trial NCT00108355 about?

NCT00108355 is a clinical study titled "Vasoconstrictors as Alternatives to Albumin After Large-Volume Paracentesis (LVP) in Cirrhosis". 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.

What is the current status of trial NCT00108355?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 29 participants. The study started on 2003-12. Estimated completion is 2012-08.

What conditions does trial NCT00108355 study?

This clinical trial studies the following conditions: Cirrhosis, Ascites.

What interventions are being tested in trial NCT00108355?

The interventions under investigation include: Midodrine (DRUG), Octreotide LAR (DRUG), Albumin (DRUG), Intravenous Saline Infusion (Albumin placebo) (DRUG), Oral tablet (Midodrine placebo) (DRUG).

Who is sponsoring clinical trial NCT00108355?

This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00108355 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cirrhosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00108355's enrollment target sits among peer trials

29 42nd of 53 higher than 12 of 53 other Cirrhosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cirrhosis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00108355, the US trial registry maintained by the National Library of Medicine. NCT00108355 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.