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The Pleth Variability Index and Hypotension at Caesarean Under Spinal.

Sponsor
Sheffield Teaching Hospitals NHS Foundation Trust (Other)
Overall Status
Completed
CT.gov ID
NCT02285569
Collaborator
(none)
17
Enrollment
1
Location
6
Duration (Months)
2.8
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

During a caesarean section the blood pressure is usually measured every few minutes and it may fall too quickly to be detected in a timely fashion by this intermittent means. The monitor the Masimo Rainbow SET® (MRS) uses a peg attached to a finger to detect (amongst other things) the flow of blood through it. One of the measures it takes is called the Pleth Variability Index (PVI) which (unlike standard blood pressure measurement) it measures continuously. The investigators would like to try the MRS on patients to see if the PVI can be used to predict falls in blood pressure.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    BACKGROUND: When a baby is delivered by a surgical procedure (a Caesarean Section) the women will usually have a spinal anaesthetic. With a spinal anaesthetic local anaesthetic is injected into the spinal fluid to make the woman numb from her chest to her feet and this allows her to be comfortable but awake during the birth. One of the common side effects of a spinal anaesthetic is that the woman's blood pressure may fall making her feel unwell and (rarely) causing stress to the unborn baby. During a caesarean section the blood pressure is usually measured every few minutes and it may fall too quickly to be detected in a timely fashion by this intermittent means. The monitor the Masimo Rainbow SET® (MRS) uses a peg attached to a finger to detect (amongst other things) the flow of blood through it. One of the measures it takes is called the Pleth Variability Index (PVI) which (unlike standard blood pressure measurement) it measures continuously. The investigators have used the MRS on one of their patients who was having a caesarean section under a spinal anaesthetic and the PVI was seen to change before the patients blood pressure fell. Because this was only one case they would like to try the MRS on some more patients to see if the PVI can be used to predict falls in blood pressure. To keep a close eye on the blood pressure they would use another monitor called a finometer. A finometer measures blood pressure continuously by means of a small cuff that is placed around a finger. The finometer should allow them to follow changes in blood pressure more closely and see how these affect the PVI reading.

    AIMS: The aim of this study is to see whether changes in PVI happen before a fall in blood pressure when a woman is having a spinal anaesthetic for a caesarean section.

    METHODOLOGY: The women will have exactly the same anaesthetic as they would have had if they were not in the study. The investigators will simply be using two pieces of equipment (the MRS and the Finometer) to see what happens when and if the blood pressure falls.

    EXPECTED OUTCOMES: The investigators hope that they will find that the PVI changes before the blood pressure falls significantly.

    IMPLICATIONS: If this study were to be promising then the investigators could go on to perform another study where they use the MRS to help them decide when to give drugs and intravenous fluids to stop the blood pressure from falling.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    17 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Can Changes in the Pleth Variability Index be Used to Predict Significant Hypotension During Spinal Anaesthesia for Caesarean Section?
    Study Start Date :
    Jun 1, 2014
    Actual Primary Completion Date :
    Dec 1, 2014
    Actual Study Completion Date :
    Dec 1, 2014

    Outcome Measures

    Primary Outcome Measures

    1. The primary outcome is the Pleth Variability Index change prior to a 20% fall in systolic blood pressure during spinal anaesthesia for a caesarean section. [intraoperative]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 55 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with a singleton uncomplicated pregnancy presenting for elective caesarean section under spinal anaesthesia where surgery and anaesthesia are anticipated to be uncomplicated.
    Exclusion Criteria:
    • Age under 18
    Conditions which may impair the ability of the technology to read accurately such as:

    • Reduced peripheral perfusion e.g. Raynaud's phenomenon

    • Circulating pigments e.g. bilirubin

    • Nail varnish that cannot be removed

    • Diseases of pregnancy: e.g. pregnancy induced hypertension

    • Significant coexisting maternal disease - e.g. congenital heart disease

    • Inability to speak fluent English

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Jessop Wing Hospital Sheffield South Yorkshire United Kingdom S10 2SF

    Sponsors and Collaborators

    • Sheffield Teaching Hospitals NHS Foundation Trust

    Investigators

    • Principal Investigator: Ian Wrench, Dr, Sheffield Teaching Hospitals NHS Foundation Trust

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Sheffield Teaching Hospitals NHS Foundation Trust
    ClinicalTrials.gov Identifier:
    NCT02285569
    Other Study ID Numbers:
    • STH16496
    First Posted:
    Nov 7, 2014
    Last Update Posted:
    May 27, 2015
    Last Verified:
    May 1, 2015
    Additional relevant MeSH terms:
    Hypotension

    Study Results

    No Results Posted as of May 27, 2015