Adductor Under Sartorial Canal Catheter (KTT) Versus Femoral Catheter (KTF) in a Quick Rehabilitation Process After Total Knee Replacement

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

44 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-31

Study Completion Date

2018-11-11

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The main objective of this study is to show that postoperative Total Knee Replacement (TKR), an analgesic perineural catheter in position under sartorial (KTSS) best preserves motor quadriceps femoral perineural catheter that (KTF) infused with even low doses of local anesthetics, this motor being evaluated by a semi quantitative simple clinical test locking of the knee feasible at the bedside.

Patients will be randomized in two arms:

* catheter in position under sartorial (experimental group)
* femoral catheter (control group)

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Early Ambulation After Adductor Canal Block for Total Knee Arthroplasty

NCT01459861

Pain Osteoarthritis

TERMINATED NA

The Appropriate Level of Continuous Adductor Canal Block in Patients Undergoing Total Knee Arthroplasty (TKA)

NCT04206150

Degenerative Arthritis

COMPLETED NA

Efficacy Testing of Different Tourniquet Pressure Used for Postoperative Pain Reduction in Total Knee Arthroplasty

NCT03931837

Osteoarthritis, Knee

UNKNOWN NA

Effectiveness of a Femoral Block Following Total Knee Arthroplasty (TKA)

NCT00659087

Total Knee Arthroplasty

COMPLETED PHASE4

Tourniquet vs. Short Time Tourniquet in Primary Robotic Assisted TKA

NCT03942939

Knee Arthropathy

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Total Knee Replacement

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

under sartorial catheter

catheter under sartorial

Group Type EXPERIMENTAL

under sartorial catheter

Intervention Type DEVICE

femoral catheter

Group Type OTHER

femoral catheter

Intervention Type DEVICE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

under sartorial catheter

Intervention Type DEVICE

femoral catheter

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Major Patient (≥ 18 years)
* Before tricompartmental benefit from knee replacement (TKR) unilateral,
* TKR programmed on one of the first three days of the week (Monday to Wednesday)
* Physical status score I-III,
* Non septic programmed surgery under general anesthesia
* Able to understand the protocol
* Written informed consent
* Social Insured
* Opportunity to be followed under the Protocol

Exclusion Criteria

* Age ≥ 85 years
* Obesity (BMI ≥ 35)
* Revision TKR,
* Patients not cooperating or not including the French,
* Difficulties in understanding and evaluating the score pain (VAS),
* Preoperative cognitive dysfunction making unreliable interrogation
* Patient unable to read and / or write (literacy, ...)
* Known bleeding disorders,
* Vascular surgery for femoral vessels on the operated side,
* Neuropathy of the lower limb,
* Localized infection at the puncture catheters,
* Known allergy to ropivacaine,
* Renal and / or severe hepatic impairment,
* Taking opioids for more than a month before surgery,
* Intolerance to morphine,
* Rheumatic inflammatory disease,
* Patients receiving immunosuppressive therapy or long-term corticosteroid
* Allergy or against-indications to standard treatments administered intraoperative and postoperative
* Flexion deformity\> 10 ° or valgus deformity with significant
* Refused to participate
* Patient trusteeship, guardianship, deprived of liberty
* Women premenopausal who become pregnant

Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No