Clinical Trials Directory

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UnknownNCT02311608

Effects of Terlipressin When Usual Somatostatin or Octreotide Dose Fails

Comparative Effectiveness Research: Effects of Terlipressin When Usual Somatostatin or Octreotide Dose Fails to Treat the Patients With Acute Variceal Bleeding

Status
Unknown
Phase
Study type
Observational
Enrollment
1,320 (estimated)
Sponsor
Shanghai Zhongshan Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

To observe and access the Effects and safety of terlipressin or high dose somatostatin/octreotide when usual dose somatostatin/octreotide fail to achieve hemostasis in patients with acute variceal bleeding.

Detailed description

The prognosis information of the patients with acute variceal bleeding will be collected, including hemostasis rate, early rebleeding rate, mortality, complications, severity adverse events, economic burdens and quality of life, when terlipressin or high dose somatostatin/octreotide is used as salvation to patients fail to achieve initial hemostasis.The results may help gastroenterologists to make decisions when administering vasoactive medicines to those suffered from acute variceal bleeding.

Conditions

Interventions

TypeNameDescription
DRUGTerlipressinadministered as a first-line medicine or as salvage
DRUGUsual Dose Somatostatin/Octreotideadministered as a first-line medicine or as salvage
DRUGHigh Dose Somatostatin/Octreotideadministered as salvage

Timeline

Start date
2014-02-01
Primary completion
2016-02-01
Completion
2016-06-01
First posted
2014-12-08
Last updated
2014-12-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02311608. Inclusion in this directory is not an endorsement.