Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07526831

Comparison of the Analgesic Efficacy of Adductor Canal Block and Combined Adductor Canal Block Plus IPACK Block in Knee Surgery

Comparison of the Analgesic Efficacy of Adductor Canal Block Versus Adductor Canal Block Combined With Local Anesthetic Infiltration Between the Popliteal Artery and the Capsule of the Knee (IPACK) in Patients Undergoing Knee Surgery

Status
Recruiting
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
TC Erciyes University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To evaluate the effectiveness of Adductor Canal Block and combined Adductor Canal plus IPACK block in reducing postoperative pain and analgesic requirements in patients undergoing knee surgery.

Detailed description

In total knee arthroplasty, ultrasound-guided Adductor canal block or Adductor Canal block combined with local anesthetic infiltration between the popliteal artery and the capsule of the knee (IPACK) will provide adequate postoperative analgesia.

Conditions

Interventions

TypeNameDescription
PROCEDUREAdductor Canal Block Group (Group I)All patients in Group I will receive a preoperative adductor canal block. In all groups, an intravenous patient-controlled analgesia device containing morphine will be administered for postoperative pain management.
PROCEDUREAdductor Canal + iPACK Block Group (Group II)"All patients in Group II will receive a preoperative adductor canal block combined with an iPACK block. Postoperatively, all patients in both groups will be provided with intravenous patient-controlled analgesia containing morphine for pain management.

Timeline

Start date
2026-04-15
Primary completion
2028-04-15
Completion
2028-05-01
First posted
2026-04-13
Last updated
2026-04-13

Locations

2 sites across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07526831. Inclusion in this directory is not an endorsement.