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The Effect of Cryotherapy on Postoperative Bleeding, Pain, and Anxiety Following Total Knee Arthroplasty

The Effect of Cryotherapy on Postoperative Bleeding, Pain, and Anxiety in Older Adults Following Total Knee Arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170313033047N4
Enrollment
76
Registered
2025-11-15
Start date
2025-11-21
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Total Knee Arthroplasty.

Interventions

Intervention 1: Intervention group: All patients will receive routine care according to the physician’s recommendations. The intervention will commence immediately after the surgical procedure and ret

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Participants with cognitive health, indicated by a score greater than 7 on the Abbreviated Mental Test (AMT) Patients undergoing total knee arthroplasty Stable physiological status, with vital signs within the normal range according to the patient’s condition and the physician’s judgment, enabling the participant to respond to questions Ability to communicate verbally and fully understand the Persian language

Exclusion criteria

Exclusion criteria: Presence of any clinical condition that, according to the attending physician, would limit or contraindicate the use of cryotherapy Having alcohol and drug addiction Having psychological disorders recorded in the file Patients with adverse reactions to cold, including signs of cold hypersensitivity or cold intolerance Patients with severe postoperative complications, including major bleeding or acute cardiovascular problems Change in clinical condition, such as disease progression according to the physician’s judgment, or death of the patient Discharge from hospital, requirement for reoperation, or transfer from the recovery unit to other hospital wards Fever with a body temperature greater than 38°C during the intervention

Design outcomes

Primary

MeasureTime frame
Postoperative bleeding volume. Timepoint: one day prior to surgery and six hours postoperatively. Method of measurement: Blood hemoglobin levels.;Pain. Timepoint: At baseline, 12 hours, and 24 hours post-intervention. Method of measurement: Visual Analoge pain Scale.;Anxiety. Timepoint: At baseline, 12 hours, and 24 hours post-intervention. Method of measurement: Hospital Anxiety and Depression Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam jadid-Milani

Shahed University

milani@shahed.ac.ir+98 21 5121 2159

Outcome results

None listed

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