Continuous Non-invasive Assessment of Blood Pressure in Bariatric Surgery

NCT03184285 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2017-06-12

No results posted yet for this study

Summary

Comparability of discontinuous non-invasive (sphygomanometric) and continuous semi-invasive and invasive (Masimo© ; Nexfin© Monitoring ; FloTrac© Edwards Lifesciences) beat to beat measurement methods for the determination of arterial blood pressure in patients undergoing bariatric surgery.

Conditions

  • Bariatric Surgery
  • Arterial Blood Pressure

Interventions

PROCEDURE

baseline alert 1

measurement in supine position

PROCEDURE

Anti-Trendelenburg-position (ATB)

measurement under ATB

PROCEDURE

ATB in narcosis

measurement under ATB in narcosis

PROCEDURE

baseline in narcosis 1

measurement in supine position in narcosis

PROCEDURE

passive leg raising

measurement under passive leg raising

PROCEDURE

volume bolus substitution

measurement in supine position after volume bolus (15 ml/kgKG Sterofundin balanced solution intravenous)

PROCEDURE

baseline in narcosis 2

measurement in supine position

PROCEDURE

start capnoperitoneum

measurement in supine position

PROCEDURE

ATB plus capnoperitoneum

measurement under ATB plus capnoperitoneum

PROCEDURE

ATB plus capnoperitoneum plus volume bolus substitution

measurement in ATB plus capnoperitoneum after volume bolus (15 ml/kgKG Sterofundin balanced solution intravenous)

PROCEDURE

ATB loss of capnoperitoneum

measurement under ATB

PROCEDURE

baseline

measurement in supine position

PROCEDURE

baseline alert 2

measurement in supine position

PROCEDURE

torso position rising 30° at the beginning

measurement in the recovery unit

PROCEDURE

torso position rising 30° at the end

measurement in the recovery unit

Sponsors & Collaborators

  • University Hospital Schleswig-Holstein

    lead OTHER

Principal Investigators

  • Jochen Renner, PD Dr.

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-01
Primary Completion
2017-06-01
Completion
2017-06-01

Countries

  • Germany

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 NCT03184285 on ClinicalTrials.gov