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Clinical Trials/NCT03620942
NCT03620942
Active, not recruiting
Not Applicable

Development of Advanced Double Intravenous Vasopressor Automated (ADIVA) System With Improved Hemodynamic Trend Control During Spinal Anaesthesia for Caesarean Section

KK Women's and Children's Hospital1 site in 1 country173 target enrollmentNovember 7, 2018

Overview

Phase
Not Applicable
Intervention
Phenylephrine
Conditions
Hypotension
Sponsor
KK Women's and Children's Hospital
Enrollment
173
Locations
1
Primary Endpoint
Number of events of Hypotension occurrence
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

Maternal hypotension during spinal anaesthesia for Caesarean delivery may bring various adverse effects. It is therefore important to closely monitor hypotension during spinal anaesthesia, however current technology does not allow the blood pressure monitoring to respond in timely manner should there be any occurrence of hypotension. The investigators developed an advanced double-intravenous vasopressor automated system (ADIVA) so as to tackle this issue via novel algorithm to control blood pressure more rigorously with more stable haemodynamic profiles.

Detailed Description

The incidence of maternal hypotension during spinal anaesthesia for Caesarean delivery is reported to be as high as 70-90%. The potential adverse effects resulting from maternal hypotension are nausea, vomiting, cardiac dysfunction, foetal acidosis and hypoxia. Hypotension during spinal anaesthesia is currently detected using an intermittent blood pressure (BP) monitor cycling and reactive administration of vasopressors upon detection. The use of conventional non-invasive BP monitoring is limited by the time required to inflate and to deflate the cuffs commonly applied to the arm, which subsequently leads to a failure to react in a timely manner to BP changes when they occur. The DIVA system (double-intravenous vasopressor automated system) previously developed helped tackle the limitations associated with the conventional management of hypotension in Caesarean sections under spinal anaesthesia. In a recent randomized controlled trial the DIVA system achieved less incidence of maternal hypotension compared to conventional management, however the side effects in mother and baby were still not fully eliminated. In this proposed study a new algorithm for an advanced DIVA (ADIVA) system will be developed to control BP more rigorously by detecting BP with more stable haemodynamic profiles and thereby improve patient outcomes. The clinical trial will be conducted in 2 phases. The first phase included the use of ADIVA in 76 subjects who undergo spinal anaesthesia for Caesarean delivery to test its safety and efficacy. The second phase was a randomised controlled trial to investigate the use of ADIVA in comparison to the existing DIVA system in 97 patients undergoing spinal anaesthesia for Caesarean section.

Registry
clinicaltrials.gov
Start Date
November 7, 2018
End Date
December 31, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
KK Women's and Children's Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy adult (American Society of Anesthesiologists physical status 1 and 2) parturients;
  • With singleton full-term pregnancy;
  • The indication for an elective cesarean delivery;
  • The use of spinal anaesthesia for cesarean delivery;
  • Anthropometric profile within the following range: age 21-50 years old, weight 40-90 kg and height of 145-170 cm.

Exclusion Criteria

  • Obstetric (e.g. pre-eclampsia, premature rupture of amniotic membranes for more than 48 hours, gestational diabetes on insulin, pregnancy-induced hypertension on medication) and uncontrolled medical (e.g. cardiac disease) complications;
  • Contraindication to spinal anaesthesia and/or allergy to opioids.

Arms & Interventions

ADIVA system

Vasopressor delivery automated system administering phenylephrine and ephedrine using a three-step algorithm vasopressor delivery technique

Intervention: Phenylephrine

ADIVA system

Vasopressor delivery automated system administering phenylephrine and ephedrine using a three-step algorithm vasopressor delivery technique

Intervention: Ephedrine

ADIVA system

Vasopressor delivery automated system administering phenylephrine and ephedrine using a three-step algorithm vasopressor delivery technique

Intervention: ADIVA System

DIVA system

Vasopressor delivery automated system administering phenylephrine and ephedrine using a two-step algorithm vasopressor delivery technique

Intervention: Phenylephrine

DIVA system

Vasopressor delivery automated system administering phenylephrine and ephedrine using a two-step algorithm vasopressor delivery technique

Intervention: Ephedrine

DIVA system

Vasopressor delivery automated system administering phenylephrine and ephedrine using a two-step algorithm vasopressor delivery technique

Intervention: DIVA System

Outcomes

Primary Outcomes

Number of events of Hypotension occurrence

Time Frame: 1 day (during cesarean delivery)

Systolic blood pressure less than 80% of baseline systolic blood pressure

Secondary Outcomes

  • Number of events of Hypertension occurrence(1 day (during cesarean delivery))
  • Number of events of Nausea and vomiting occurrence(1 day (during and after cesarean delivery))

Study Sites (1)

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