Comparison of Epidural Analgesia With Intra-Articular Infiltration Analgesia

Namik Kemal University

Status: Not yet enrolling

Conditions: Local Infiltration; Epidural; Analgesia

Treatments: Other: Recording the amount of medication and the number of complications according to observational follow-up

Study type: Interventional

Funder types: Other

Identifiers

NCT06872528

NamikKU-AGultekin-2

Details and patient eligibility

About

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.

Enrollment: 30 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Age range 18-75
2. Those who underwent surgery with combined spinal anesthesia
3. Drugs administered with combined spinal anesthesia and intra-articular infiltration analgesia

Exclusion criteria

1. Those who do not want to participate in the study
2. Those who underwent surgery under general anesthesia
3. Patients outside the specified age range
4. Patients with inadequate follow-up results (patient, drug and device related)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

---

30 participants in 2 patient groups

Analgesia provided only with epidural analgesia

Active Comparator group

Treatment:

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

Analgesia provided with epidural analgesia and local infiltration

Active Comparator group

Treatment:

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