Analgesia
Procedure1- Real Adductor canal block + surgical infiltration and sham of femoro-cutaneous block + obturator block + IPACK block with physiological serum
NCT Number: NCT06920186
The aim of this study is to evaluate the analgesic efficacy of this quadruple sensory block compared with the currently recommended procedure (adductor canal block + infiltration).
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Hôpital Privé Claude Galien, Quincy-sous-Sénart, France
In addition to the adductor canal block, this quadruple block incorporates :
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1- Real Adductor canal block + surgical infiltration and sham of femoro-cutaneous block + obturator block + IPACK block with physiological serum
Time frame: From enrollement to the last H24 after surgery
The QoR-15 score at H24 after surgery was compared between the two groups for primary endpoint analysis.
The QoR-15 accurately measures postoperative recovery by focusing on 5 key domains: pain, physical comfort, physical independence, psychological support and emotional state. Each item is rated from 0 (unfavorable) to 10 (favorable), with an overall score corresponding to the sum of the score obtained for each item, i.e. a score from 0 (no recovery) to 150 (full recovery).
Time frame: Hour 0
Functional assessment of the knee with KOOS JR questionnaire
Time frame: Hour 2
Pain measured with a simple numeric scale
Time frame: Hour 6
Pain measured with a simple numeric scale
Time frame: Hour 12
Pain measured with a simple numeric scale
Time frame: Hour 12
time between end of intervention and first ambulation
Time frame: Hour 24
Pain measured with a simple numeric scale
Time frame: Hour 24
Measurement of the joint range of both knees
Time frame: Hour 24
time between end of intervention and first ambulation
Time frame: Hour 48
Pain measured with a simple numeric scale
Time frame: Hour 48
Quality of recovery measured with QoR 15 questionnaire
Time frame: Hour 48
Opioid drug use evaluation
Time frame: Hour 48
Non-opioid drug use evaluation
Time frame: Hour 48
Measurement of the joint range of both knees
Time frame: Hour 48
time between end of intervention and first ambulation
Time frame: Hour 48
Length of stay in the post-intervention monitoring room
Time frame: Month 1
Pain measured with a simple numeric scale
Time frame: Month 1
Measurement of the joint range of both knees
Time frame: Month 1
Length of hospitalisation
Time frame: Month 1
Time taken for the patient to return to their usual activities
Time frame: Month 1
Drug tolerance
Time frame: Hour 1
Patient comfort during loco-regional anesthesia
Time frame: Month 1
Functional assessment of the knee with KOOS JR questionnaire
GCS Ramsay Santé pour l'Enseignement et la Recherche
Other
Comparison of the Benefit of Peripheral Nerve Quadri-block Versus Adductor Canal Block + Surgical Infiltration in Total Knee Arthroplasty
Acronym: INCA
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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