NCT02018068

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

60
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2014

Typical duration for not_applicable

Geographic Reach
3 countries

4 active sites

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 10, 2013

Completed
13 days until next milestone

First Posted

Study publicly available on registry

December 23, 2013

Completed
22 days until next milestone

Study Start

First participant enrolled

January 14, 2014

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 27, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 27, 2016

Completed
Last Updated

July 10, 2018

Status Verified

July 1, 2018

Enrollment Period

2.5 years

First QC Date

December 10, 2013

Last Update Submit

July 6, 2018

Conditions

Keywords

Patient-controlled Perineural analgesiaPostoperativeOrthopedic surgery"Remote Control" versus "at bedside care"Comparative medico-economic evaluation

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

EXPERIMENTAL

For 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.

Other: Remote control

At bedside care

ACTIVE COMPARATOR

For 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".

Other: 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.

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.

At bedside care

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Anesthesia Réanimation Department, Hôpital Saint Roch

Nice, 06001, France

Location

A Schweitzer Hospital

Dordrecht, Netherlands

Location

Rachid Hospital

Dubai, United Arab Emirates

Location

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.

MeSH Terms

Conditions

Foot InjuriesPain, Postoperative

Condition Hierarchy (Ancestors)

Leg InjuriesWounds and InjuriesPostoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Officials

  • Xavier XC CAPDEVILA, MD, PhD

    CHU Montpellier - Department of Anesthesiology and critical care, Lapeyronie University Hospital

    PRINCIPAL INVESTIGATOR

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

Locations