Comparison of Epidural Analgesia With Intra-Articular Infiltration Analgesia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorNamik Kemal University

About this trial

The results of combining infiltrative analgesia applied by orthopedists with epidural analgesia applied by anesthesiologists after knee replacement surgery will be compared.

It aims to compare epidural analgesia with the maximum reduction of postoperative pain in patients, as well as in terms of both analgesic and complications.

The study will include patients who have undergone knee replacement surgery for six months. In the study, we will compare the results of painkillers applied to the patient from the waist or knee after the waist numbing anesthesia, which includes some of the routinely applied protocols of your knee replacement surgery. It is a condition that will be monitored after surgery. The study aims to reduce maximum pain with two painkiller methods applied in small amounts or together. No interventional application will be made to the patient who will undergo surgery other than routine application. After the surgery, you will be asked verbally about your pain level and side effects at certain hours after the surgery and the amount of painkillers used and the amount of painkillers will be determined according to the follow-up hours (1st, 2nd, 6th, 12th, 24th and 48th hours after the surgery). In addition to these, complications will also be monitored. The results of patients who can be fully followed up at the end of 6 months will be presented as a scientific study.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age range 18-75

Those who underwent surgery with combined spinal anesthesia

Drugs administered with combined spinal anesthesia and intra-articular infiltration analgesia

Disqualifiers

Those who do not want to participate in the study

Those who underwent surgery under general anesthesia

Patients outside the specified age range

Patients with inadequate follow-up results (patient, drug and device related)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Recording the amount of medication and the number of complications according to observational follow-up

    Other intervention

    Observational monitoring of patients and recording data for 24 hours

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Analgesia provided only with epidural analgesiaActive comparator 1 intervention
Group B: Analgesia provided with epidural analgesia and local infiltrationActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Amount of local anesthetic used for epidural analgesia

Is there a statistical difference between the two groups? Monitoring the effect of local infiltration on the amount of epidural analgesic agent

Time frame
6 months
2

Differences between the two groups in terms of complications and need for additional analgesia

The effect of epidural analgesia and infiltration analgesia on complications and additional analgesia needs in patients

Time frame
6 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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