Viewing Study NCT06201195



Ignite Creation Date: 2024-05-06 @ 7:59 PM
Last Modification Date: 2024-10-26 @ 3:17 PM
Study NCT ID: NCT06201195
Status: COMPLETED
Last Update Posted: 2024-06-07
First Post: 2023-10-25

Brief Title: Anterior Cutaneus Nerve and Distal Adductor Canal Block With USG for Total Knee Replacement Analgesia
Sponsor: Diskapi Teaching and Research Hospital
Organization: Diskapi Teaching and Research Hospital

Study Overview

Official Title: Contribution of Anterior Femoral Cutaneous Nerve Block to Postoperative Analgesia for Total Knee Replacement
Status: COMPLETED
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to compare analhesia effects of adductor canal blockade versus distal adductur canal blockade added anterior cutaneus nerve block in total knee arthroplasty

The main questions it aims to answer are

question 1 does distal adductor canal blockade anterior cutaneus nerve blokade superior analgesia then adductor canal block for undergoing TKP
question 2 does distal adductor canal blockade anterior cutaneus nerve blokade decrease drain place pain on anterolateral face of knee
Detailed Description: Patients with American Society of Anesthesiologists classification status I-III scheduled for elective primary TKA using standard spinal anesthesia enroll for this trial After surgery patient divided two groups 1- adductor canal blockade 2- distal adductor canal blockade anterior femoral cutaneus nerve blockade At postoperative 3th 10th 24th hour VAS visuel analouge scale VAS move incision plase pain-for top and down of patella drain place pain motor strenght for femoral nerve and siyatic nerve first analjesic requirement time opioid consumption total analcesic requirement will be recorded

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None