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Demonstrate the Effectiveness to Hemopatch in Controlling Postoperative Bleeding After Laparoscopic Cholecistectomy and in Reducing of Morbidity and Postoperative Hospital Stay

NCT02777307 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2016-05-19

No results posted yet for this study

Summary

Demonstrate the effectiveness to Hemopatch in controlling postoperative bleeding or reducing of postperative fluid collection after laparoscopic cholecistectomy, morbidity and postoperative hospital stay.

Conditions

  • Efficacy of Hemopatch in Controlling of Postoperative Bleeding or Reducing of Postperative Morbidity After Laparoscopic Cholecistectomy

Interventions

OTHER

Hemopatch Sealing Hemostat

Place of Hemopatch Sealing Hemostat after laparoscopic cholecistectomy

Sponsors & Collaborators

  • Azienda Ospedaliera San Gerardo di Monza

    collaborator OTHER

  • San Giuseppe Moscati Hospital

    collaborator OTHER

  • Ospedali Riuniti di Foggia

    collaborator OTHER

  • Ospedale Regina Apostolorum

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2016-12-31
Completion
2017-05-31

Countries

  • Italy

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 NCT02777307 on ClinicalTrials.gov