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Local Anesthetic

Continuous Nerve Block for Post-Knee Replacement Pain

N/A
Recruiting
Led By Naveed Siddiqui, MD, MSc
Research Sponsored by University of Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Patients older than 21 years of age
American Society of Anesthesiologists (ASA) physical status I-III
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 90
Awards & highlights

Study Summary

This trial aims to see if using a continuous nerve block during total knee arthroplasty can improve outcomes and pain management compared to single shot nerve blocks.

Who is the study for?
This trial is for patients over 21 years old who are having knee replacement surgery as outpatients and have a moderate risk of complications (ASA I-III). They should not be dependent on alcohol or drugs, understand the treatment process, and cannot be using strong painkillers regularly. People with allergies to study meds, blood clotting issues, low platelet counts, or problems where the catheter goes can't join.Check my eligibility
What is being tested?
The study tests if continuous adductor canal block (CACB), which involves infusing pain medication through a tube near nerves in the thigh, provides better pain control and recovery after outpatient knee surgery compared to a sham procedure without real medicine (ShACB).See study design
What are the potential side effects?
Potential side effects may include discomfort at the catheter site, infection risk from the tube placement, possible nerve damage around the thigh area where medication is infused, and typical reactions to local anesthetics like numbness or weakness.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am older than 21 years.
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My overall health is good to moderately impaired.
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I am having knee replacement surgery on one knee as an outpatient.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 90
This trial's timeline: 3 weeks for screening, Varies for treatment, and day 90 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Quality of Recovery 15 score (QoR-15)
Secondary outcome measures
Opioid usage
Pain scores

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Continuous adductor canal block (CACB)Experimental Treatment1 Intervention
Will receive an infusion of 0.2% ropivacaine 5mL/h through adductor canal catheter.
Group II: Sham continuous adductor canal block (ShACB).Placebo Group1 Intervention
Will receive an infusion of NaCl 0.9% 5mL/h through adductor canal catheter.

Find a Location

Who is running the clinical trial?

University of TorontoLead Sponsor
690 Previous Clinical Trials
1,019,587 Total Patients Enrolled
MOUNT SINAI HOSPITALOTHER
40 Previous Clinical Trials
14,575 Total Patients Enrolled
1 Trials studying Acute Pain
400 Patients Enrolled for Acute Pain
Naveed Siddiqui, MD, MScPrincipal InvestigatorUniversity of Toronto
1 Previous Clinical Trials
223 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many people are being enrolled in this experiment?

"Affirmative. According to information available on clinicaltrials.gov, the trial in question is actively recruiting participants since it was initially posted on October 1st, 2023 with a recent update performed October 12th of the same year. The current goal is to enrol 56 patients from one medical centre."

Answered by AI

Does this research endeavor still need volunteers?

"Affirmative. According to the clinicaltrials.gov data, this medical trial is actively looking for volunteers and was first posted on October 1st 2023 before being updated most recently on December 10th 2023. This study needs 56 patients from a single site in order to move forward."

Answered by AI
Recent research and studies
~20 spots leftby Sep 2024