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OpenTrials
Completed

NCT Number: NCT02074475

SPI Value Relevance in Clinical Practice

Primary endpoint: Defining The optimal target range for Surgical Pleth index. Surgical Pleth Index (SPI, formerly used SSI = Surgical Stress Index) is a novel multivariate index, which is based on the sum of the normalized pulse beat interval (PBI) and the photoplethysmography. SPI indicates the balance between intensity of surgical stimulation and the level of anti-nociception (opioid analgesia and neural blockade). This study is a Spin off from a larger Adequacy of Anaesthesia study and aims on finding the most appropriate target range for SPI in order to avoid signs of inadequate anaesthesia. Patients are treated without monitoring adequacy of anaesthesia thus the values are collected blinded and analyzed afterwards in accordance of signs for inadequate anaesthesia. The study population will be 150 patients.

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Key information

Conditions

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Tampere University Hospital

Tampere, 33521, Finland

About this study

Signs of non-adequate anaesthesia are motor and/or autonomic nervous system arousals during surgery.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ability to provide written informed consent
  • Age 18-80 years of age
  • Surgery that is expected to last at least 2 hours under general anesthesia with endotracheal tube

Exclusion criteria

  • Any subject that meets the definition of vulnerable subject as defined in ISO 14155:2011o Per ISO 14155:2011, a vulnerable subject is defined as an individual whose willingness to volunteer in a clinical investigation could be unduly influenced by the expectation, whether justified or not, of benefits associated with participation or of retaliatory response from senior members of a hierarchy in case of refusal to participate
  • Any subject with a cardiac pacemaker
  • Any subject with atrial fibrillation at the time of obtaining the baseline values
  • Any subject with more than 5 ventricular extra systoles/minute at the time of obtaining the baseline values
  • Any subject who needs invasive blood pressure measurement
  • Any subject who show hemodynamics that would have qualified for being considered as a sign of inadequate anesthesia already at baseline:

o Mean blood pressure below 60 mmHg or above 100 mmHg o HR below 45 /min or above 100/min

  • Any subject with epidural anesthesia or analgesia during the surgery. Epidural catheter may be placed pre-operatively, and used in the PACU, but not during the surgery
  • Any subject having surgery that requires prone position
  • Any subject with very high body mass index (>35) because of incompatibility with the target controlled anesthesia models used
  • Any subject with known allergies to the specific anesthetic agents/ analgesic drugs intended for use in their surgeries
  • Any subject with laryngeal mask airway
  • Any subject who requires neuromuscular blocking agent infusion
  • Any subject who is going to have major surgery with a high risk of extensive blood loss
  • Any subject with known chronic use of opioids

Treatment and study plan

Control Group

Other

A group of no Monitoring patients from larger AoA study with no adequacy of anaesthesia monitoring

Primary outcomes

  1. optimal maximum limit for SPI

    Time frame: 1 day

    SPI -value at a predefined criteria for signs of anaesthesia.

Secondary outcomes

  1. Optimal lower limit for SPI

    Time frame: 1 day

    The measured lower limit SPI-value at the time point for signs of too deep anaesthesia

Sponsors and collaborators

Lead sponsor

Tampere University Hospital

Other

Registry information

Official study title

GE AOA Study Spin-off: Defining the Clinically Useful Range for Surgical Pleth Index

Acronym: SPIrelevance

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Feb 28, 2014
Registry last updated
May 5, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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