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NOT YET RECRUITING
NCT06942702
NA

Efficacy of Genicular Block on Total Knee Arthroplasty Surgery

Sponsor: Mersin University

View on ClinicalTrials.gov

Summary

The aim of this study is to investigate the postoperative pain relieving effect of preoperative genicular block in total knee arthroplasty surgery. The main questions it aims to answer are: 1. Do visual analog scale (VAS) scores decrease in patients who underwent geniculate block? 2. Does opioid consumption decrease in patients who underwent geniculate block? Researchers will compare postoperative pain in patients who received genicular block with those who did not.One group of patients will be administered 0.25% bupivacaine with the geniculate block method. The other group will not undergo any intervention. Both groups will be administered intravenous morphine for postoperative analgesia.

Official title: Assesment of Postoperative Analgesic Efficacy of Preoperatively Applied Genicular Block on Total Knee Arthroplasty: A Randomized Controlled Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

44

Start Date

2025-12-20

Completion Date

2026-12-20

Last Updated

2025-12-23

Healthy Volunteers

No

Interventions

DRUG

Genicular blocks (bupivakain)

Genicular block is a regional analgesic technique performed with USG

DRUG

Patient Control Analgesia (PCA) Morphine group

this group consists of the patients no any intervention preoperatively and they will be given morfin with PCA (Patient controlled analgesia) and paracetamol 3x1000 mg intravenous and diclofenac 75 mg intramuscular (if needed)

DRUG

Paracetamol (acetaminophen) + Diclofenac Sodium

All patients are given paracetamol (3x1000 mg) and diclofenac (if needed)