Adductor Canal Block Versus Parasartorial Compartment Block for Pain Relief and Recovery After Arthroscopic Knee Surgery

Comparison of the Effects of Adductor Canal Block and Parasartorial Compartment Block on Postoperative Analgesia and Functional Recovery After Arthroscopic Knee Surgery: A Prospective, Randomized, Double-Blind Study

Status

Not yet recruiting

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07790393

Enrollment

Registered

2026-08-27

Start date

2026-09-01

Completion date

2027-06-01

Last updated

2026-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain After Arthroscopic Knee Surgery

Keywords

Adductor Canal Block, Postoperative Pain, Parasartorial Compartment Block

Brief summary

The goal of this clinical trial is to compare adductor canal block and parasartorial compartment block for pain relief and functional recovery in adults undergoing elective arthroscopic knee surgery. The main questions it aims to answer are: Which block provides better pain relief at rest and during movement 24 hours after surgery? How do the two blocks compare in opioid use, muscle strength, knee movement, early walking, side effects, and patient satisfaction? Researchers will compare participants who receive an adductor canal block with those who receive a parasartorial compartment block to determine whether one technique provides better pain relief and functional recovery while preserving muscle strength. Participants will: Be randomly assigned to receive either an ultrasound-guided adductor canal block or an ultrasound-guided parasartorial compartment block Have their pain at rest and during knee movement assessed for 48 hours after surgery Have their opioid use, quadriceps muscle strength, knee movement, walking ability, side effects, and satisfaction evaluated after surgery

Interventions

DRUGMeperidine

If the patient's NRS is 4 or more, 0.5 mg/kg meperidine will be given

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Scheduled for elective unilateral primary arthroscopic knee surgery

Exclusion criteria

* Revision or bilateral arthroscopic knee surgery * Surgery performed for trauma or an emergency indication * Contraindications to regional nerve block, including infection at the injection site, coagulopathy, or inappropriate anticoagulant use * Allergy to amide-type local anesthetics * Pre-existing peripheral neuropathy or motor deficit in the limb to be operated on * Dysfunction of the contralateral limb severe enough to interfere with functional assessments * Chronic opioid use * Severe cognitive impairment * Pregnancy or lactation

Design outcomes

Primary

Measure	Time frame	Description
Pain at Rest 24 Hours After Surgery	24 hours	Pain intensity at rest will be assessed using the Numeric Rating Scale, ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Lower scores indicate less pain.

Countries

Turkey (Türkiye)

Contacts

CONTACTFatma P Ucar, MD

fpinarucar@gmail.com+905377697281

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 28, 2026