Vital-signs-integrated Patient-assisted Intravenous Opioid Analgesia (VPIAmorphine)
Primary Purpose
Respiratory Depression
Status
Active
Phase
Phase 2
Locations
Singapore
Study Type
Interventional
Intervention
VPIA analgesia
Morphine
Sponsored by
About this trial
This is an interventional treatment trial for Respiratory Depression focused on measuring Respiratory Depression
Eligibility Criteria
Inclusion Criteria:
- Age 21-70 years old, female
- Healthy participants who are American Society of Anesthesiologists physical status 1 and 2 (with well controlled medical problems)
- Undergoing elective surgery with the intent of using postoperative PCA with morphine for postoperative analgesia
Exclusion Criteria:
- Allergy to morphine
- With significant respiratory disease and obstructive sleep apnea
- Unwilling to place oxygen saturation monitoring devices during study period
- Unable to comprehend the use of patient controlled analgesia
- Pregnant
Sites / Locations
- KK Women's and Children's Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
VPIA analgesia system
Arm Description
Vital-signs-integrated patient-assisted intravenous opioid analgesia system (VPIA). The vital signs (oxygen saturation, respiratory rate, heart rate) will be close monitored when patients is using VPIA pump. The drug used is intravenous morphine (1mg per milligram) with bolus of 1 mg.
Outcomes
Primary Outcome Measures
Number of episodes of breech in safety thresholds
Any episode of oxygen saturation <95%, Heart rate <60 bpm or Respiratory rate <8 breaths/min
Secondary Outcome Measures
Pain scores
Visual pain score 0-10
Full Information
NCT ID
NCT02804022
First Posted
February 28, 2016
Last Updated
August 8, 2023
Sponsor
KK Women's and Children's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02804022
Brief Title
Vital-signs-integrated Patient-assisted Intravenous Opioid Analgesia
Acronym
VPIAmorphine
Official Title
Vital-signs-integrated Patient-assisted Intravenous Opioid Analgesia for Postsurgical Pain: A Novel Modality to Improve Patient Safety by Detecting and Preventing Respiratory Depression
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 29, 2016 (Actual)
Primary Completion Date
May 30, 2017 (Actual)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
KK Women's and Children's Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a closed-loop system which is embodied in a novel and intelligent algorithm that takes into account patients' vital signs. The system allows better and responsive titration of personalized pain relief together with non-invasive physiological monitoring that measures oxygenation, breathing and heart rate continuously.
Detailed Description
A glaring safety gap in the administration of commonplace Patient Controlled Analgesia (PCA) opioids unfortunately exists. A significant proportion of patients may suffer from respiratory depression with the use of PCA opioids and it is imperative to discover solutions to improve the safety of PCA opioids, therein improving medication safety, enhancing quality of postoperative care and providing economic cost savings. Currently, no continuous monitoring system that integrates an intelligent decision making response exists.
The investigators primary aim is to develop and commercialise a Vital-signs-integrated (using oxygen saturation, respiratory rate, heart rate) Patient-assisted Intravenous opioid Analgesia (VPIA) that can be integrated into the hospital-wide monitoring systems is capable of making intelligent decision making responses to bridge the PCA safety gap within 12 months.
This VPIA delivery system will be a closed-loop system for safety and efficacy. It will be integrated with continuous vital signs monitoring, and provide appropriate response to breach of safety parameters. It will be part of a larger surveillance system that provides tiered medical and nursing alerts to safety parameters.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Depression
Keywords
Respiratory Depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
VPIA analgesia system
Arm Type
Experimental
Arm Description
Vital-signs-integrated patient-assisted intravenous opioid analgesia system (VPIA). The vital signs (oxygen saturation, respiratory rate, heart rate) will be close monitored when patients is using VPIA pump. The drug used is intravenous morphine (1mg per milligram) with bolus of 1 mg.
Intervention Type
Device
Intervention Name(s)
VPIA analgesia
Other Intervention Name(s)
VPIA delivery system
Intervention Description
Recruited subjects will be given a VPIA device containing 1mcg/ml of morphine. Morphine will be administered via an intravenous infusion line with an anti-reflux valve to ensure precise drug administration and no backflow.
Intervention Type
Drug
Intervention Name(s)
Morphine
Other Intervention Name(s)
Morphine-VPIA
Intervention Description
Recruited subjects will be given a VPIA device containing 1mcg/ml of morphine. Morphine will be administered via an intravenous infusion line.
Primary Outcome Measure Information:
Title
Number of episodes of breech in safety thresholds
Description
Any episode of oxygen saturation <95%, Heart rate <60 bpm or Respiratory rate <8 breaths/min
Time Frame
2 days
Secondary Outcome Measure Information:
Title
Pain scores
Description
Visual pain score 0-10
Time Frame
2 or 3 days
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Only female patients undergoing elective surgery in this institution will be recruited. The study site is specialised in providing healthcare only to women and children in Singapore.
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 21-70 years old, female
Healthy participants who are American Society of Anesthesiologists physical status 1 and 2 (with well controlled medical problems)
Undergoing elective surgery with the intent of using postoperative PCA with morphine for postoperative analgesia
Exclusion Criteria:
Allergy to morphine
With significant respiratory disease and obstructive sleep apnea
Unwilling to place oxygen saturation monitoring devices during study period
Unable to comprehend the use of patient controlled analgesia
Pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ban L Sng, FANZCA
Organizational Affiliation
KK Women's and Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
KK Women's and Children's Hospital
City
Singapore
ZIP/Postal Code
229899
Country
Singapore
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32513113
Citation
Sng BL, Tan DJ, Tan CW, Han NR, Sultana R, Sia ATH. A preliminary assessment of vital-signs-integrated patient-assisted intravenous opioid analgesia (VPIA) for postsurgical pain. BMC Anesthesiol. 2020 Jun 8;20(1):145. doi: 10.1186/s12871-020-01060-4.
Results Reference
derived
Learn more about this trial
Vital-signs-integrated Patient-assisted Intravenous Opioid Analgesia
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