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NCT07416721

Cooling of the Knee After Total Knee Arthroplasty

Not yet recruiting NA Last updated 18 February 2026
What this trial tests

NA trial testing Cool Down Liquid with Bandage ( CoolDown, CH) in Osteoarthritis, Knee in 99 participants. Not yet recruiting.

Timeline
1 March 2026
Primary endpoint
1 November 2026
1 March 2027

Quick facts

Lead sponsorClinical Center of Vojvodina
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment99
Start date1 March 2026
Primary completion1 November 2026
Estimated completion1 March 2027

Drugs / interventions tested

Conditions studied

Sponsor

Clinical Center of Vojvodina

Who can join

Eligibility, any sex, with Osteoarthritis, Knee or Total Knee Replacement. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study investigates whether cooling the knee after total knee replacement surgery can reduce pain and improve early recovery. After surgery, patients are randomly assigned to one of three groups: cooling with a liquid cooling bandage, cooling with an ice pack, or standard postoperative care without cooling. Cooling begins 24 hours after surgery and continues for two weeks. Pain levels, use of pain medication, blood values, knee swelling, knee movement, and length of hospital stay are recorded. The goal is to determine whether postoperative knee cooling provides additional benefits compared with standard care.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Osteoarthritis, Knee

Currently open trials in the same condition.

Other Clinical Center of Vojvodina trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07416721.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing