Development of Advanced Double Intravenous Vasopressor Automated (ADIVA) System

Anesthesia Clinical Trial

— ADIVA  

Official title:

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03620942
• Other study ID #: SHF/CTG061/2017
• Status: Active, not recruiting
• Phase: N/A
• Start date: November 7, 2018
• Est. completion date: December 31, 2024

Study information

• Verified date: November 2022
• Source: KK Women's and Children's Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 173
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 21 Years to 50 Years

Eligibility

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.

Related Conditions & MeSH terms

• Anesthesia
• Hypotension

Intervention

Drug:
• Phenylephrine
Phenylephrine will be administered with conditions as below: When systolic blood pressure is between 90-110% of baseline, 25mcg phenylephrine will be given either in infusion or bolus if heart rate = 60 beats/min; When systolic blood pressure is less than 90% of baseline, 25 to 75mcg phenylephrine will be given either in infusion or bolus if heart rate = 60 beats/min.
• Ephedrine
Ephedrine will be administered with conditions as below: When systolic blood pressure is between 90-110% of baseline, 2mg ephedrine will be given either in infusion or bolus if heart rate < 60 beats/min; When systolic blood pressure is less than 90% of baseline, 2 to 6mg ephedrine will be given either in infusion or bolus if heart rate < 60 beats/min.

Device:
• ADIVA System
When systolic blood pressure (SBP) is 100-110% of baseline, 25mcg phenylephrine (infusion) is given if heart rate = 60 beats/min, and 2mg ephedrine (infusion) is given if heart rate < 60 beats/min; When SBP is 90-100% of baseline, 25mcg phenylephrine (infusion or bolus) is given if heart rate = 60 beats/min, and 2mg ephedrine (infusion or bolus) is given if heart rate < 60 beats/min; When SBP is 80-90% of baseline, 50mcg phenylephrine (infusion or bolus) is given if heart rate = 60 beats/min, and 4mg ephedrine (infusion or bolus) is given if heart rate < 60 beats/min; When SBP < 80% of baseline, 75mcg phenylephrine (infusion or bolus) is given if heart rate = 60 beats/min, and 6mg ephedrine (infusion or bolus) is given if heart rate < 60 beats/min.
• DIVA System
DIVA system works as below: When systolic blood pressure is between 90 to 100% of baseline, 25mcg phenylephrine (bolus) will be given if heart rate = 60 beats/min, whereas 2mg ephedrine (bolus) will be given if heart rate < 60 beats/min; When systolic blood pressure is less than 90% of baseline, 50mcg phenylephrine (infusion or bolus) will be given if heart rate = 60 beats/min, whereas 4mg ephedrine (infusion or bolus) will be given if heart rate < 60 beats/min.

Locations

Country	Name	City	State
Singapore	KK Women's and Children's Hospital	Singapore

Sponsors (1)

Lead Sponsor	Collaborator
KK Women's and Children's Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of events of Hypotension occurrence	Systolic blood pressure less than 80% of baseline systolic blood pressure	1 day (during cesarean delivery)
Secondary	Number of events of Hypertension occurrence	Systolic blood pressure more than 120% of baseline systolic blood pressure	1 day (during cesarean delivery)
Secondary	Number of events of Nausea and vomiting occurrence	Nausea and vomiting during and after cesarean delivery	1 day (during and after cesarean delivery)