Arthroplasty Clinical Trial
Official title:
Does the Measurement of Pupillary Reactivity to Painful Stimulation by an Automated Pupillometer Determine the Effectiveness of Local Anesthesia When Undergoing General Anesthesia?
The pupillary pain-meter AlgiScan ® with integrated nociceptive stimulator is a portable,
battery-operated device which automatically measures, by means of an infrared camera, pupil
diameter. This is measured in response to noxious stimulation produced by a tetanus at a
frequency of 100 Hz for 5 seconds. Its intensity varies from 10 to 60 mA. The recording is
performed for a period of 13 seconds (3 seconds prior to stimulation, stimulation for 5
seconds, 5 seconds after the stimulation). An interval of 3 minutes is allowed between the
two measurements (right and left), which is significantly higher than the time necessary to
return to normal (about 20seconds).
The pupillary pain index (PPI) ranges from 0 to 10 and is a composite measure of the
pupillary diameter reflex to the tetanus stimuli delivered by the AlgiScan device. Smaller
scores indicate increased analgesia.
The main objective of this study is to determine whether PPI index variation can determine a
prognostic threshold of analgesic efficacy of unilateral lower limb sensory nerve block
before incision. The measurements are performed after bilateral nociceptive stimulation
(blocked side versus non-blocked side) in patients under general anesthesia for major knee
surgery.
The secondary objectives of this study are to find a link between the clinical criteria for
block failure and the ratio of the blocked side PPI over the unblocked side PPI:
- study the potential link between algic thermal sensitivity (tested prior to general
anesthesia) and the blocked side PPI (or the asymmetry of the index between the blocked
side and the unblocked side).
- study the potential link between postoperative morphine consumption and the blocked
side PPI index (or the asymmetry of the index between the blocked side and the
unblocked side).
- study the potential link between consumption of remifentanil during surgery and the
blocked side PPI index (or the asymmetry of the index between the blocked side and the
unblocked side).
- study the potential link between the hemodynamic response to incision and the blocked
side PPI index (or the asymmetry of the index between the blocked side and the
unblocked side).
- study the potential link between morning pain assessment and the blocked side PPI index
(or the asymmetry of the index between the blocked side and the unblocked side).
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Diagnostic
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
NCT06323980 -
INHANCE Stemless Reverse Shoulder IDE
|
N/A | |
| Completed |
NCT00762944 -
Total Temporomandibular Joint Replacement System Post Approval Study
|
||
| Not yet recruiting |
NCT05015101 -
Evaluation of the Clinical and Radiological Outcome of Uncemented Femoral Stems According to Their Proximal Coating
|
||
| Completed |
NCT02554149 -
Radiological Measurement of Femoral Stem Version Using Lateral Decubitus Method: A Prospective Study
|
N/A | |
| Terminated |
NCT02713906 -
Materialise X-ray Knee Guides for Total Knee Arthroplasty
|
N/A | |
| Recruiting |
NCT02828293 -
Understanding GMK Sphere Implant Tibiofemoral Kinematics by Means of Dynamic Videofluoroscopy
|
||
| Completed |
NCT02829866 -
AMIStem-H Radiographic Analysis
|
||
| Terminated |
NCT00683267 -
Efficacy and Safety Study of 4975 in Patients Undergoing Total Hip Replacement
|
Phase 2 | |
| Completed |
NCT04516239 -
Comparison of Metal on Metal Total Hip Arthroplasty and Metal on Metal Total Hip Resurfacing.
|
Phase 4 | |
| Recruiting |
NCT04480320 -
Sonography-guided Pericapsular Never Group Block for Hip Arthroplasty
|
N/A | |
| Not yet recruiting |
NCT04906681 -
Implementation of a Rehabilitation Technology in Orthopedic and Neurological Rehabilitation to Increase Therapy Dosage: an Exploratory Study
|
Phase 1/Phase 2 | |
| Completed |
NCT04403919 -
Knotless Suture in Revision Total Joint Arthroplasty
|
N/A | |
| Completed |
NCT03132831 -
Influence of the Operative Day on the Average Duration of Stay in Primary Hip and Knee Replacements
|
||
| Active, not recruiting |
NCT03339557 -
Comparison of Three Knee Replacements
|
N/A | |
| Active, not recruiting |
NCT02578446 -
Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in Total Knee Replacement
|
N/A | |
| Not yet recruiting |
NCT00756483 -
Stability Plus - Outcomes From Extended Continuum of Care
|
N/A | |
| Terminated |
NCT00364533 -
A Study to Evaluate the Effectiveness and Safety of Tapentadol(CG5503) in the Treatment of Acute Pain After Hip Replacement Surgery Compared With Oxycodone and Placebo Followed by a Voluntary Open-Label Extension For Safety
|
Phase 3 | |
| Terminated |
NCT04089371 -
A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) System
|
||
| Completed |
NCT05248854 -
Effects of Sensorimotor and Core Stabilization Exercises After Total Knee Arthroplasty
|
N/A | |
| Not yet recruiting |
NCT02465684 -
Effect of Tourniquet on UKA
|
N/A |