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Effect of Prostacyclin on Haemostasis in Abdominal Surgery

NCT01528943 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2021-03-10

No results posted yet for this study

Summary

The purpose of this study is to investigate the effect of continuous perioperative infusion of prostacyclin on haemostasis and endothelial functionality in patients undergoing major abdominal surgery.

Conditions

  • Surgery

Interventions

DRUG

Prostacycline

Continuous infusion peri -and 6 hours postoperatively of prostacycline 1 ng/kg/min

DRUG

Isotonic saline

same volume as the group that are allocated to prostacycline

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    lead OTHER

Principal Investigators

  • Pär Johansson I Johansson, MD DMSc MPA · Professor

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2013-03-31
Completion
2014-01-31

Countries

  • Denmark

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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 NCT01528943 on ClinicalTrials.gov