Skip to content

Analgesic efficacy comparison between the dual subsartorial block and local infiltration analgesia following total knee replacement: A randomized controlled trial.

Analgesic efficacy comparison between the dual subsartorial block and local infiltration analgesia following total knee replacement: A randomized controlled trial.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250919004
Enrollment
66
Registered
2025-09-19
Start date
2025-11-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Advanced osteoarthritis of the knee in patients who required unilateral total knee replacement. dual subsartorial block, local infiltration analgesia, postoperative pain control, total knee replacement, knee osteoarthritis, multimodal analgesia

Interventions

In this group, the surgeon will perform LIA for the operated knee with the cocktail regimen composed of bupivacaine 200 mg plus ketorolac 60 mg and adrenaline 0.03 mg diluted with NSS to a total of 15
Active Comparator Procedure/Surgery,Experimental Procedure/Surgery
LIA,DSB

Sponsors

Faculty of Medicine, Khon Kaen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients who plan to undergo unilateral TKR under spinal anesthesia 2. Age over 18 years 3. ASA physical status 1-3

Exclusion criteria

Exclusion criteria: 1. Refuse to participate 2. Previous knee surgery or redo-surgery 3. Allergy or contraindicate to study drugs, paracetamol, morphine, ketorolac, or bupivacaine 4. Body weight less than 35 kg 5. PNB contraindications include skin infection at the block site, and coagulopathy 6. Inability to cooperate, communicate, or report pain scores.

Design outcomes

Primary

MeasureTime frame
postoperative pain score at 24 hour after surgery postoperative at PACU, 6h, 12h, 24h, 36h, and 48h. Numeric rating pain score (patient self-report their pain intensity using 11-point scale from 0-10)

Secondary

MeasureTime frame
postoperative morphine consumption postoperative at PACU, 6h, 12h, 24h, 36h, and 48h. total morphine consumption (mg)

Countries

Thailand

Contacts

Public ContactPuntira Chitto

Faculty of Medicine, Khon Kaen University

puntira40@gmail.com043363060

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026