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Clinical Trials/NCT06651762
NCT06651762CompletedNot Applicable

Ultra Sound Guided Genicular Nerves Cooled Radiofrequency Ablation in Total Knee Replacement Surgeries

Ain Shams University1 site in 1 country66 target enrollmentStarted: October 14, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
66
Locations
1
Primary Endpoint
o Epidural rescue doses

Study Overview

Brief Summary

Total Knee Replacement surgery is common procedure that is usually done for patients suffering from persistent pain with limitation of movement. Unfortunately, they do suffer after the operation as it is associated still with significant pain that affect the rehabilitation plan, hospital length of stay, life style and patient satisfaction. New approaches are rising every day to add to the multimodal management plan. Genicular nerves cooled radiofrequency ablation is a new approach that can be simply done U.S. guided with little side effects, if any, and great results.

Detailed Description

the study measures the efficacy of genicular nerves cooled radiofrequency ablation in enhancing quality of rehabilitation in patients undergoing total knee replacement

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Undergoing a scheduled unilateral total knee replacement surgery

Exclusion Criteria

  • •• Allergy to any of the drugs used in the study
  • •Alcohol or drug abuse
  • •Psychiatric disease

Arms & Interventions

lumber Epidural and unilateral genicular nerve ablation:

Experimental

Patient will receive lumber epidural anesthesia and unilateral genicular nerve cooled radio frequency ablation pre-operative

Intervention: unilateral Radiofrequency (Procedure)

lumber epidural anesthesia

Experimental

Patients will receive epidural anesthesia intra operative

Intervention: Epidural (Procedure)

lumber Epidural and unilateral genicular nerve ablation:

Experimental

Patient will receive lumber epidural anesthesia and unilateral genicular nerve cooled radio frequency ablation pre-operative

Intervention: Epidural (Procedure)

Epidural and bilateral genicular nerve ablation

Experimental

Patient will receive lumber epidural anesthesia and bilateral genicular nerve cooled radio frequency ablation pre-operative

Intervention: bilateral Radiofrequency (Procedure)

Epidural and bilateral genicular nerve ablation

Experimental

Patient will receive lumber epidural anesthesia and bilateral genicular nerve cooled radio frequency ablation pre-operative

Intervention: Epidural (Procedure)

Outcomes

Primary Outcomes

o Epidural rescue doses

Time Frame: 1st 48 hours

rescue doses reflects degree of pain control

Secondary Outcomes

  • WOMAC score(baseline preoperative, and the at 2, 6 and 12 weeks postoperative)
  • Knee range of motion(Assessed weekly for 3 weeks postoperatively (Weeks 1, 2, and 3))
  • Postoperative inflammatory signs assessed by clinical examination(Assessed weekly for 3 weeks postoperatively (Weeks 1, 2, and 3).)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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