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THE EFFECTIVENESS OF THERMOELECTRIC ICE PACK TO REDUCE POSTOPERATIVE PAIN AFTER TOTAL KNEE REPLACEMENT

THE EFFECTIVENESS OF THERMOELECTRIC ICE PACK TO REDUCE POSTOPERATIVE PAIN AFTER TOTAL KNEE REPLACEMENT

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260424005
Enrollment
60
Registered
2026-04-24
Start date
2025-04-01
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

Postoperative pain after total knee replacement Osteoarthritis, Knee Arthroplasty, Replacement, Knee Pain, Postoperative Cold Packs Thermoelectric Devices

Interventions

Patients in the experimental group receive standard postoperative pain management, including routine analgesic medications, plus thermoelectric ice pack application to the operated knee. The device is
Experimental Device,Active Comparator Device
Thermoelectric ice pack,Conventional gel cold pack

Sponsors

Mahidol university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Male or female patients diagnosed with primary knee osteoarthritis and scheduled for unilateral or bilateral total knee replacement surgery. 2. Able to communicate in Thai (speaking, reading, and writing). 3. For patients aged 60 years and older, Mini-Cog score greater than 3.

Exclusion criteria

Exclusion criteria: 1. Patients receiving analgesic drugs for other chronic pain conditions unrelated to knee osteoarthritis (e.g., cancer pain, radicular pain from herniated disc). 2. Patients transferred to an intensive care unit after surgery or who die during study participation. 3. Patients undergoing knee surgery due to trauma or malignant disease. 4. Patients with knee deformity greater than 20 degrees. 5. Patients with revision surgery of the same knee. 6. Patients with a history of rheumatoid arthritis. 7. Patients with a history of allergy to cold packs or materials used in the packs. 8. Patients with infection at the surgical site. 9. Patients with abnormal peripheral circulation (e.g., peripheral arterial or deep venous occlusive disease, vasculitis). 10. Patients diagnosed with psychiatric disorders such as schizophrenia, acute bipolar disorder, or severe major depressive disorder.

Design outcomes

Primary

MeasureTime frame
Postoperative pain intensity (NRS) Preoperative, immediately postoperative, 6, 24, 48, 72 Numeric Rating Scale (0-10), patient-reported score

Secondary

MeasureTime frame
Time to First Ambulation After Total Knee Arthroplasty From end of surgery until first ambulation Time (hours) from end of surgery to first ambulation, recorded by nursing staff using patient medical records

Countries

Thailand

Contacts

Public ContactChonnikan Sratongin

Kamphaeng Saen Hospital and Faculty of Nursing, Mahidol University

kaweped@gmail.com0901390805

Outcome results

None listed

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