Intraoperative Noradrenaline to Control Arterial Pressure (INPRESS Study)

Sponsor
University Hospital, Clermont-Ferrand (Other)
Overall Status
Completed
CT.gov ID
NCT01536470
Collaborator
Aguettant laboratory (Other)
300
1
2
52
5.8

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate whether a preventive strategy of intraoperative arterial hypotension using noradrenaline can reduce the incidence of postoperative organ failure.

Condition or Disease Intervention/Treatment Phase
  • Other: noradrenaline
  • Other: Ephedryne chorydrate
Phase 4

Detailed Description

The maintenance of arterial blood pressure is essential for organ perfusion pressure. Intraoperative hypotension is a frequent complication both after induction and during maintenance of anaesthesia, ranging from 5% to 75% depending on the chosen definition. Tissue hypoperfusion exposes to the occurrence of a systemic inflammatory response syndrome and is a key determinant of postoperative complications. Persistent intraoperative hypotension has been reported as an important prognostic factor of postoperative morbidity and mortality. Adequate treatment of arterial hypotension is therefore of particular importance during surgery, but optimal strategy of intraoperative blood pressure management remains undetermined, especially in high-risk patients. Target ranges for arterial pressure are not clearly defined, and hypotension is usually defined as a systolic pressure of less than 80 mmHg or a decrease of more than 40% from baseline.

Traditionally, management of intraoperative hypotension consisted primarily of fluid administration whereas vasoconstrictors, such as Ephedrine chlorhydrate, are often used as a second line therapy. This may, however, expose patients to prolonged hypotension and to excessive fluid administration, and each of them may alter tissue oxygenation.

Recent experimental data have shown that noradrenaline, which has - and -adrenergic effects, has no detrimental effects on microcirculatory blood flow and tissue oxygenation in the intestinal tract. Because of anaesthesia-induced vasodilatation, the use of a continuous infusion of noradrenaline to increase systemic vascular resistance could be useful to prevent detrimental effects of compromised tissue perfusion, especially in high-risk surgical patients.

The primary objective of the study is to compare two strategies of intraoperative blood pressure management in high-risk surgical patients: 1- Continuous infusion of noradrenaline to maintain arterial blood pressure of no more than 10% below its baseline value; 2- Conventional treatment of hypotension (defined as a blood pressure of below 80 mmHg or a decrease of more than 40% from baseline) using intravenous bolus of Ephedrine chorhydrate.

The investigators hypothesis is that maintenance of arterial blood pressure with noradrenaline could reduce postoperative organ dysfunction in high-risk surgical patients.

Study Design

Study Type:
Interventional
Actual Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effectiveness of Noradrenaline to Control Intraoperative Arterial Pressure in High-risk Surgical Patients: A Multicentre Prospective Randomized Controlled Trial
Study Start Date :
Mar 1, 2012
Actual Primary Completion Date :
Jul 1, 2016
Actual Study Completion Date :
Jul 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Noradrenaline

Continuous infusion of noradrenaline to maintain arterial blood pressure management in high-risk surgical patients

Other: noradrenaline
The primary objective of the study is to compare two strategies of intraoperative blood pressure management in high-risk surgical patients: 1- Continuous infusion of noradrenaline to maintain arterial blood pressure of no more than 10% below its baseline value; 2- Conventional treatment of hypotension (defined as a blood pressure of below 80 mmHg or a decrease of more than 40% from baseline) using intravenous bolus of Ephedrine chorhydrate.

Experimental: Ephedrine chorhydrate

Conventional treatment of hypotension (defined as a blood pressure of below 80 mmHg or a decrease of more than 40% from baseline)using intravenous bolus of Ephedrine chorhydrate

Other: Ephedryne chorydrate

Outcome Measures

Primary Outcome Measures

  1. Composite endpoint of postoperative SIRS and at least one major organ dysfunction [day-7]

Secondary Outcome Measures

  1. Incidence of intraoperative hypotension [at day 7]

  2. Incidence of intraoperative hypertension [at day 7]

  3. Incidence of intraoperative bradycardia [at day 7]

  4. Intraoperative volume of fluid perfused [at day 7]

  5. Intraoperative blood losses [at day 7]

  6. Need for intraoperative transfusion [at day 7]

  7. Postoperative organ failure [at day 7]

  8. Biologic criteria: plasma concentration of NGAL, creatinine, CRP, serum lactate, troponine) [at day 7]

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age ≥ 50 years

  • ASA score ≥ 2

  • Planned and unplanned surgical procedures

  • Abdominal, orthopaedic and vascular surgery

  • Expected duration ≥ 2 hours

  • AKI risk index ≥ class 3

Exclusion Criteria:
  • Severe preoperative hypertension (not controlled)

  • Creatinine clearance < 30 ml/min or preoperative dialysis

  • Acute cardiac failure

  • Preoperative sepsis

  • Preoperative hemodynamic failure (shock)

  • Intraoperative use of locoregional anaesthesia (epidural and spinal)

  • Patient refusal

  • Pregnancy and/or lactation

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Clermont-Ferrand Clermont-Ferrand France 63003

Sponsors and Collaborators

  • University Hospital, Clermont-Ferrand
  • Aguettant laboratory

Investigators

  • Principal Investigator: Emmanuel FUTIER, University Hospital, Clermont-Ferrand

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Clermont-Ferrand
ClinicalTrials.gov Identifier:
NCT01536470
Other Study ID Numbers:
  • CHU-0111
  • 2011-004232-66
First Posted:
Feb 22, 2012
Last Update Posted:
Oct 3, 2016
Last Verified:
Sep 1, 2016
Keywords provided by University Hospital, Clermont-Ferrand
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 3, 2016