Postoperative Patient-controlled Perineural Analgesia After Orthopedic Surgery by "Remote Control" Versus "Bedside Care"
MICREL
1 other identifier
interventional
72
3 countries
4
Brief Summary
Perineural injection of local anesthesic is currently the reference method for the treatment of post operative pain in a patient undergoing major orthopedic surgery. Postoperative pain is a dynamic phenomena in every patient. It is classified as intense during the first postoperative hours after surgery, and decreases in a non-linear manner over the days following the procedure. PCA (patient control analgesia) infusion of local anesthesic allows an adaptation of the local analgesia doses to the evaluated pain scores, as well as permit a decrease in adverse events related to the continuous infusion technique (motor or sensory blockade, paresthesia, etc.). The physician can also modify the pump settings according to the postoperative rehabilitation plan.The use of new communication techniques such as "telemedecine" may be of interest in reducing treatment onset time and optimizing pain management. The remote control consists to change the settings of the pump after if the anesthesiologist was informed in real time (via a smartphone or a tablet) on patient pain level, sensory and motor blockades. The physician goes to a dedicated website (Micrel CareTM). and makes the necessary changes by remote control via a GPRS (General Packet Radio Service) connexion. The aim of this prospective, comparative, multicentric trial is to compare the effectiveness of patient management through two communication modalities: remote control versus bedside care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2014
Typical duration for not_applicable
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 10, 2013
CompletedFirst Posted
Study publicly available on registry
December 23, 2013
CompletedStudy Start
First participant enrolled
January 14, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 27, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
July 27, 2016
CompletedJuly 10, 2018
July 1, 2018
2.5 years
December 10, 2013
July 6, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Time between the patient's call and the change in Patient Control Analgesia (PCA) pump settings
from arriving at the ward after surgery until 72 postoperative hours
Secondary Outcomes (10)
Number of nursing interventions
from arriving at the ward after surgery until 72 postoperative hours
Duration of nursing interventions
from arriving at the ward after surgery until 72 postoperative hours
Post operative pain measured by VAS (Visual Analog Scale)
from before implementation of PCA until 72 postoperative hours
Amount of rescue analgesia
from implementation of PCA (Patient Control Analgesia) until 72 postoperative hours
Patient satisfaction Score at catheter removal (at 72 postoperative hours)
at 72 postoperative hours
- +5 more secondary outcomes
Study Arms (2)
Remote control
EXPERIMENTALFor patient randomized in arm "Remote Control", the communication with anesthesiologist will be done by teletransmission. The intervention "Remote control" is assigned to this arm. When evaluated pain values, sensory or motricity blockades are over the selected threshold then, the patient enters the data in the PCA (Patient Control Analgesia) pump, the physician in charge of the patient for the protocol is alerted by SMS on a specific smart phone and makes the necessary settings changes by Remote Control on the Micrel CareTM site.
At bedside care
ACTIVE COMPARATORFor patient randomized in arm "At bedside care", the communication with the anesthesiologist in charge of the patient will be done via the nurses and referent physician of the medical unit, as a routine procedures. The necessary changes of pump settings are doing by the anesthesiologist. The intervention "at beside care" is assigned to arm "at bedside care".
Interventions
When pain or sensory and motor block evaluation exceed the thresholds, the patient enters the data in the PCA (patient Control Analgesia) pump. The investigator is alerted by SMS on his smartphone and makes the necessary programming changes by remote control on the Micrel Care TM site. Systematic assessments via the PCA pump are scheduled for 9:00, 13:00 and 19:00 every day during 48 to 72 hours. The patient can alert his physician through his PCA pump of any additional requests (pain, motor blockade, numbness). The anesthesiologist receives an SMS alert and can make any necessary programming changes to the pump via the remote control.
When pain or sensory and motor block evaluation exceed the thresholds, the nurse contacts the physician and she will be able to modify the pump settings according to the anesthesiologist prescription. The delay between the call of the patient and the programming changes, the duration of the procedure are reported. Systematic evaluations via the PCA (Patient Control Analgesia) pump are done when the patient arrives in this surgical ward and at 9:00, 13:00 and 19:00 every day for 48 to 72 hours.Throughout the study, if necessary, the nurse or referring physician performs the programming changes directly on the PCA pump and notes the delay in treatment. All the reasons and the duration of any bedside visit are reported.
Eligibility Criteria
You may qualify if:
- Patients scheduled for elective orthopedic surgery
- Patients older than 18 years old
- Patient with a surgical indication (foot, shoulder or knee) which can require placement of a perineural catheter
- Patients classified ASA class I to III
- Informed consent
You may not qualify if:
- Contraindication to regional anesthesia or local anesthetics
- Contraindication to paracetamol, ketoprofen or morphine (depending on the selected rescue analgesia)
- Hospital discharge less than 48 hours after surgery
- Psychomotor disease (teletransmission contraindication)
- Patient undergoing surgery with a duration greater than 4 hours
- Patient with a duration of perineural catheter less than 48 hours
- Protected patient
- Patient enrolled in another study
- Patient who can't understand local language
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (4)
Department of Anesthesiology and critical care, Lapeyronie University Hospital
Montpellier, 34295, France
Anesthesia Réanimation Department, Hôpital Saint Roch
Nice, 06001, France
A Schweitzer Hospital
Dordrecht, Netherlands
Rachid Hospital
Dubai, United Arab Emirates
Related Publications (1)
Capdevila X, Macaire P, Bernard N, Biboulet P, Cuvillon P, Choquet O, Bringuier S. Remote transmission monitoring for postoperative perineural analgesia after major orthopedic surgery: A multicenter, randomized, parallel-group, controlled trial. J Clin Anesth. 2022 May;77:110618. doi: 10.1016/j.jclinane.2021.110618. Epub 2021 Dec 1.
PMID: 34863052DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xavier XC CAPDEVILA, MD, PhD
CHU Montpellier - Department of Anesthesiology and critical care, Lapeyronie University Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 10, 2013
First Posted
December 23, 2013
Study Start
January 14, 2014
Primary Completion
July 27, 2016
Study Completion
July 27, 2016
Last Updated
July 10, 2018
Record last verified: 2018-07