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Perineural Dexamethasone in the Adductor Canal Block

Perineural Dexamethasone in the Adductor Canal Block for Postoperative Pain in Knee Arthroplasty Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06079047
Enrollment
66
Registered
2023-10-12
Start date
2023-12-15
Completion date
2025-10-31
Last updated
2025-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Pain

Keywords

knee arthroplasty, glucocorticoids, adductor canal block

Brief summary

Postoperative pain management in total knee arthroplasty (TKA) surgery is a real challenge for the anesthesiologist. Effective pain control must be provided while preserving the mobility to ensure early rehabilitation. The adductor canal block is an effective way to induce sensory block without motor block. However, the major disadvantage of this block is the duration of sensory block which may be insufficient for postoperative pain management in TKA surgery. Many studies have focused on finding molecules that can prolong sensory block without the need for a perineural catheter and dexamethasone is among the most studied molecules(1, 2). Hence, our study aims to evaluate the added value of perineural dexamethasone in the adductor canal block in TKA surgery. \[

Detailed description

Using a computer-generated sequence of random numbers, the patients included will be randomly allocated to get an adductor canal block using : Group D: 10 ml of 0.5% bupivacaine + 10 ml of 0.9% normal saline solution + 8 mg of dexamethasone (equivalent to 2 ml) Group C: 10 ml of 0.5% bupivacaine + 10 ml of 0.9% normal saline solution + 2 ml of 0.9% normal saline solution All patients included in the study will initially be evaluated at the anesthesia outpatient clinic with correction of any existing health issues. A pre-anesthesia visit will be conducted the day before the procedure for all patients, providing them with information about the protocol of our study and obtaining their consent to participate. Upon arrival at the operating room, non-invasive monitoring of blood pressure, pulse oximetry, and ECG tracing will be performed and also a blood glucose level measurement. An 18-gauge peripheral intravenous line will be established, and 0.03 mg per kg midazolam was administrated. All patients will receive spinal anesthesia. Depending on the patient's condition, investigators will opte for: A single shot spinal anesthesia using 0.5% bupivacaine (11 mg) with fentanyl (25 µg) for patients under 65 years of age with ASA I and II Continuous spinal anesthesia with drug titration for patients over 65 years of age or with ASA III classification. None of patients will receive intravenous dexamethasone during the perioperative period. The decision to use a tourniquet and use of cement will be left to the surgeon. In the immediate postoperative period, all patients will receive an adductor canal block with a high-frequency probe. The patients will be positioned in a supine position with the leg slightly externally rotated. The probe will be placed transversely on the inguinal fold. The femoral vessels (artery and vein) will be identified. The different muscular structures delimiting the adductor canal will be visualized: the sartorius muscle that covers the femoral artery and the medial vastus muscle laterally. The saphenous nerve, which is usually hyperechoic, is located most often at the lateral edge of the artery in the fascia between the sartorius and medial vastus muscles. A 100 mm neurostimulation needle was used and 22 ml solution was injected into the adductor canal. Patients will be transferred to continuous care unit for 48 hours. Post operative analgesia will include: 1. Paracetamol 1g IV every 6 hours for 1 day then oral paracetamol 1g every 8 hours for 4 weeks 2. Diclofenac sodium (50 mg) \*2 per day for 5 days 3. PCA morphine (Patient Controlled Analgesia), as a rescue analgesia. The first rise will be allowed on day 1 (18 h postoperatively) and the patient will be asked to wander with a walking frame for a distance of at least 3 meters (about 10 steps). The patient will be considered ready for discharge after completing protocol endpoints and walking at least 3 meters without support.

Interventions

Adductor canal block with dexamethasone

PROCEDUREgroup Controle

Adductor canal block with saline solution

Sponsors

Olfa kaabachi, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients scheduled for unilateral TKA * Surgery under spinal anesthesia * ASA class I, II, and III patients

Exclusion criteria

* Patient refusal to participate in the study * Contraindication to regional anesthesia * Allergies to the products used * Bilateral TKA * Revision TKA * TKA in the context of inflammatory or post-traumatic disease * BMI \> 45 * Poorly controlled diabetic patients with HbA1c \> 8% * Patients on corticosteroid therapy or who have received an intra-articular injection of corticosteroids

Design outcomes

Primary

MeasureTime frameDescription
morphine consumption48 hourspostoperative consumption of morphine

Secondary

MeasureTime frameDescription
NRS on mouvement1 hour, 3 hous, 6 hours, 9 hours,12 hours, 24 hours, 36 houes and 48 hours postoperativelyNumerical rate scale during knee flexion \[ NRS =0 no pain ; NRS =10 worse pain\]
knee mouvementpreoperatively, on day 1 and day 7 postoperativelyRange of mouvement of the knee
walkday 1 and day 2 postoperativelyNumbers of steps
Patient's satisfaction48 hours postoperatively3 level scale :0: not satisfied; 1: mild satisfaction; 2: satisfied
Blood glucose level1 hour, 6 hours,12 hours,18 hours, 24 hours postoperativelyBlood glucose level
NRS at rest1 hour, 3 hours, 6 hours, 9 hours,12 hours, 24 hours, 36 hours and 48 hours postoperativelyNumerical rate scale at rest \[ NRS =0 no pain ; NRS =10 worse pain\]
quality of recoveryday oneQoR15 score \[ 136-150 excellent recovery - 0-89 poor recovery\]
neuropathic Chronic pain6 MONTHSDN4 questionnaire \[ no neuropathic pain 0 - neuropathic pain \>4\]
chronic pain6 monthsNRS on mouvement \[ NRS =0 no pain ; NRS =10 worse pain\]
postoperative quality of life6 monthsSF-12 score \[0 to 100, with higher scores indicating better physical and mental health functioning\]
knee fonction6 monthsKOOS PS score \[\[0 to 100, with higher scores indicating better knee function\]functioning\]
pain at home7 days postoperativelyNRS at mouvement \[ NRS =0 no pain ; NRS =10 worsE pain\]

Countries

Tunisia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026