Clinical Trials Directory

Trials / Completed

CompletedNCT02122705

A Case Series of VPIA Using Remifentanil for Labour and Delivery

A Case Series of Vital Signs-controlled, Patient Assisted Intravenous Analgesia (VPIA) Using Remifentanil for Labour and Delivery

Status
Completed
Phase
Study type
Observational
Enrollment
29 (actual)
Sponsor
KK Women's and Children's Hospital · Other Government
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study is a prospective case series aiming to evaluate a new VPIA remifentanil algorithm which would benefit labouring mothers who are unable or unwilling to receive epidural analgesia.

Detailed description

This study proposes a novel Vital signs-controlled, patient-assisted intravenous analgesia (VPIA) regimen that will enhance the efficacy, safety and personalization of remifentanil therapy for labouring women. This system will study the parturient's pattern of analgesic use in 15 min epochs and titrate the demand doses and basal infusion rate to maintain a plasma level of remifentanil that is appropriate for the degree of pain felt. The system incorporates vital signs (pulse oximetry and heart rate values) into the algorithm which would temporarily stop the pumps and step down doses accordingly when predefined critical values are reached.

Conditions

Interventions

TypeNameDescription
DEVICEVPIA remifentanilVital signs controlled patient assisted intravenous analgesia using remifentanil

Timeline

Start date
2012-05-01
Primary completion
2016-01-01
Completion
2016-06-01
First posted
2014-04-24
Last updated
2017-02-07

Locations

1 site across 1 country: Singapore

Source: ClinicalTrials.gov record NCT02122705. Inclusion in this directory is not an endorsement.