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CompletedNot applicableResults posted

Ketamine Administration for Postoperative Pain Management in Patients Undergoing Knee Arthroplasty

NCT07059429 · KETARTHRO · State Budgetary Healthcare Institution, National Medical Surgical Center N.A. N.I. Pirogov, Ministry of Health of Russia

Closed to entry
Status
Not accepting participants
Not applicable
Phase
100
Target enrolment
1
Study sites
Outside the US

What it is testing

Summary

This study is conducted to evaluate the effectiveness and safety of ketamine infusion for pain relief after knee replacement surgery. Adult patients who have undergone knee arthroplasty will be randomly assigned to one of two groups. The study group will receive standard pain management plus a continuous infusion of ketamine using patient-controlled analgesia (PCA), while the control group will only receive standard pain management. All patients will be monitored for pain intensity using the Numeric Rating Scale (NRS) at several time points the first 24 hours after surgery. The study will compare the total amount of opioid pain medication required, the level of pain experienced, and the frequency and severity of side effects such as nausea, vomiting, and neuropsychiatric reactions. The goal is to determine whether adding ketamine to standard pain management reduces opioid use and improves pain control without increasing side effects. The results improve pain management strategies after knee replacement surgery.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Total Opioid Consumption in Morphine Equivalents Within 24 Hours After Surgery

    Measured over 24 hours postoperatively

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years to 90 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * Age greater than 18 years and less than 90 years. * Patients who have undergone knee arthroplasty. * The patient has read the information sheet and signed the informed consent form. Exclusion Criteria: * Spinal anesthesia performed intraoperatively. * Epidural analgesia administered postoperatively. * Perioperative blockade of the sciatic nerve, genicular nerve, or lumbar plexus. * Allergy to ketamine or non-steroidal anti-inflammatory drugs. * Contraindications to ketamine as specified in the product instructions. * Time from the end of surgery to study enrollment exceeds 24 hours. * Ineffectiveness of analgesia as provided by the study protocol.

Where

1 study site

FacilityCityRegionCountry
Pirogov National Medical and Surgical CenterMoscowRussia

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT07059429 on ClinicalTrials.gov →

Last updated in the registry 2026-03-02. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits