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Clinical Trials in Turkey / NCT07002580
Recruiting Not applicable

Evaluation of the Effectiveness of iPACK and Adductor Canal Blocks on Patients Undergoing Arthroscopic Knee Surgery

NCT07002580 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-07-01
Last updated
2026-02-06

Condition(s) studied

Patients Undergoing Arthroscopic Knee Surgery

Investigational drug(s) / intervention(s)

IPACK and adductor canal block with Bupivacaine 0.25%Spinal Anesthesia with Bupivacaine

IPACK and adductor canal block with Bupivacaine 0.25%: iPACK block is infiltration between the Popliteal Artery and the Capsule of the Knee. iPACK and adductor canal blocks are performed with ultrasound guidence under sterile conditions.

Spinal Anesthesia with Bupivacaine: Spinal Anesthesia is a basic anesthesia method used for years to grant anesthesia for surgeries for lower extremities and lower torso surgeries.

Study summary

Arthroscopic knee surgery is one of the most commonly performed procedures in orthopedic surgery. More than 50% of patients experience moderate to severe pain after the operation. Inadequate postoperative pain control and poor recovery quality can negatively impact physiotherapy protocols, prolong hospital stays, and consequently lead to cognitive dysfunction, systemic infections, and increased healthcare costs.

Therefore, reducing postoperative pain and improving recovery quality are of great importance. In our clinic, a variety of analgesic techniques are routinely employed as part of a multimodal analgesia approach for patients undergoing arthroscopic knee surgery. One of these techniques is the simultaneous application of the IPACK block and the adductor canal block.

In this study, we aim to evaluate the effectiveness of these blocks on postoperative recovery quality in patients undergoing arthroscopic knee surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged between 18 and 50 years, * Scheduled for arthroscopic knee surgery under spinal anesthesia due to knee pathology * Patients classified as ASA physical status I-II-III according to the American Society of Anesthesiologists risk classification Exclusion Criteria: * Coagulopathy * ASA IV-V patients * Uncooperable patients * Patients who refuses to participate in study * Patients who takes chronic pain treatments

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sakarya University Training and Research Hospital Sakarya Turkey (Türkiye) Recruiting

More Sakarya University trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07002580 on ClinicalTrials.gov ↗ ← All trials in Turkey