Hemospray in Gastrointestinal Bleeding: A Real-life Multicenter Cohort

NCT03611504 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 261

Last updated 2019-02-21

No results posted yet for this study

Summary

This is an observational, retrospective, analytical, and multicenter study conducted at 17 hospitals. Our research aims to assess the effectiveness of Hemospray® in patients with gastrointestinal bleeding in clinical practice. Besides, we aim to detect predictors of treatment failure defined as unsuccessful immediate hemostasis or rebleeding.

Conditions

  • Gastrointestinal Hemorrhage
  • Ulcer Hemorrhage
  • Tumor Bleeding

Interventions

DEVICE

Hemospray®

Hemospray® application

Sponsors & Collaborators

  • University of Salamanca

    collaborator OTHER
  • Hospital del Mar

    collaborator OTHER
  • Puerta de Hierro University Hospital

    collaborator OTHER
  • Complejo Hospitalario de Navarra

    collaborator OTHER
  • Hospital de Henares

    collaborator OTHER
  • Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

    collaborator OTHER
  • Quirón Madrid University Hospital

    collaborator OTHER
  • Hospital de Cruces

    collaborator OTHER
  • Hospital General Universitario Gregorio Marañon

    collaborator OTHER
  • Hospital Universitario Central de Asturias

    collaborator OTHER
  • Hospital Universitario de Cabuenes

    collaborator OTHER
  • Hospital Universitario Doctor Peset

    collaborator OTHER
  • Hospital del Rio Hortega

    collaborator OTHER
  • Hospital Universitario Madrid Sanchinarro

    collaborator OTHER
  • Hospital de Aviles

    collaborator UNKNOWN
  • Hospital IMQ Zorrozaurre

    collaborator UNKNOWN
  • Hospital Universitario Ramon y Cajal

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-01
Primary Completion
2018-12-30
Completion
2018-12-30
FDA Device
Yes

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03611504 on ClinicalTrials.gov