Status:

COMPLETED

Can Continuous Non-invasive Monitoring Improve Stability of Intraoperative Blood Pressure - A Feasibility Study.

Lead Sponsor:

University Hospital Birmingham NHS Foundation Trust

Collaborating Sponsors:

University of Warwick

Conditions:

Hip Fractures

Hypotension on Induction

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

Background During anaesthesia for repair of a broken hip, many patients experience low blood pressure. There have been many studies showing that patients who experience low blood pressure during anaes...

Eligibility Criteria

Inclusion

  • Provision of written informed consent
  • Adult patients, undergoing surgical repair of neck of femur fracture
  • Patient can understand and comprehend written and spoken English
  • Patient's consultee can understand written and spoken English

Exclusion

  • American Society of Anaesthesiologists (ASA) Class I patients
  • Patients with device-specific exclusions; atrial fibrillation, Raynauds syndrome or disease, peripheral vascular disease, scleroderma, an arteriovenous shunt, valvular heart disease.
  • Patients in whom a blood pressure cuff cannot be safely inflated on both arms for any reason (for example, lymphoedema).
  • Patients in whom the treating anaesthetist has judged they will require invasive arterial pressure monitoring.
  • Patients declining consent
  • Patients in whom the treating anaesthetist will use total intravenous anaesthesia (TIVA)
  • Patients in whom there is a \>20mmHg difference between non-invasive cuff mean arterial pressure measurements made on opposite arms.

Key Trial Info

Start Date :

June 13 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 5 2019

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT04051073

Start Date

June 13 2019

End Date

August 5 2019

Last Update

May 18 2022

Active Locations (1)

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MIDRU, Birmingham Heartlands Hospital

Birmingham, West Midlands, United Kingdom, B95SS