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Analgesic effect of esketamine as local anesthetic adjuvant for regional anesthesia in total knee arthroplasty

Analgesic effect of esketamine as local anesthetic adjuvant for regional anesthesia in total knee arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073520
Enrollment
Unknown
Registered
2023-07-13
Start date
2023-07-12
Completion date
Unknown
Last updated
2023-07-16

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

Conditions

regional anesthesia

Interventions

Medial inferior genicular nerve, 5ml 0.5% ropivacaine each). IPACK block (0.5% ropivacaine 20ml).
Ropivacaine group :Ropivacaine group: genicular nerves of knee joint (medial superior knee nerve
lateralis superior genicular nerve
Esketamine group:Esketamine group: genicular nerves of knee joint (medial superior knee nerve
Medial inferior genicular nerve, 0.5% ropivacaine 5ml+5mg esketamine in each place). IPACK block (0.5% ropivacaine 20ml+20mg esketamine).
control group:No nerve block operation

Sponsors

the First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients aged 18-90 years; ASA grades 1-3; BMI 18-40 kg/m2; A unilateral total knee arthroplasty under spinal anesthesia was planned.

Exclusion criteria

Exclusion criteria: Peripheral nerve block or contraindication to spinal anesthesia (local or systemic infection; Coagulation dysfunction; Pre-existing neurological defects or neuropathy); History of knee trauma or surgery; Any mental or mental illness that interferes with the assessment; Allergic to any component of analgesic regimens or local anaesthesia; Or chronic opioid use (=4 weeks before surgery, daily morphine equivalent dose =30mg); People with poorly controlled or untreated hypertension; Patients with untreated or undertreated hyperthyroidism.

Design outcomes

Primary

MeasureTime frame
the incidence of chronic pain;

Secondary

MeasureTime frame
Morphine consumption within 24 hours after arriving at PACU;Time required for opioid analgesics;Time to meet discharge physical therapy standards;hospital stay;Recovery Quality;Rehabilitation situation;Walking distance;

Countries

China

Contacts

Public ContactQuanguang Wang

the First Affiliated Hospital of Wenzhou Medical University

panlinmina@163.com+86 137 3693 5500

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026