Comparison Between the Effect of Infiltration Between the Popliteal Artery and Capsule of the Knee Block Versus Selective Tibial Nerve Block for Postoperative Analgesia in Patient Undergoing Total Knee Arthroplasty. A Prospective Randomized Study

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-01

Study Completion Date

2022-06-30

Brief Summary

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Comparison Between the Effect of Infiltration Between the Popliteal Artery and Capsule of the Knee Block Versus Selective Tibial Nerve Block for Postoperative Analgesia in Patient Undergoing Total Knee Arthroplasty.

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Detailed Description

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Conditions

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Postoperative Analgesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Investigators

Study Groups

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Adductor canal block with Ipack block

Group Type ACTIVE_COMPARATOR

Adductor canal block with Ipack block or selective tibial nerve block

Intervention Type PROCEDURE

Ultrasound guided

Adductor canal block with selective tibial nerve block

Group Type ACTIVE_COMPARATOR

Adductor canal block with Ipack block or selective tibial nerve block

Intervention Type PROCEDURE

Ultrasound guided

Interventions

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Adductor canal block with Ipack block or selective tibial nerve block

Ultrasound guided

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients with osteoarthritis scheduled for a primary either partial or total knee arthroplasty • Patients aged 40-80 years with a body mass index of 18-36 kg/ m2 and an American Society of Anesthesiologists functional status of I-III Planned use of regional anesthesia

Exclusion Criteria

* • Patients younger than 40 years old and older than 80years.

* Hepatic or renal insufficiency.
* Patients undergoing general anesthesia.
* Allergy or intolerance to one of the study medications.
* BMI \> 36
* Diabetes
* ASA of IV
* Chronic opioid use (taking opioids for longer than 3 months, or daily oral morphine equivalent of \>5mg/day for one month)

Minimum Eligible Age

40 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes