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The Effectiveness of ultrasound-guided Adductor Canal Block combined with IPACK (Interspace between the popliteal artery and the capsule of the posterior knee) for improve range of motion in knee arthroscopy assisted anterior cruciate ligament reconstruction

The Effectiveness of ultrasound-guided Adductor Canal Block combined with IPACK (Interspace between the popliteal artery and the capsule of the posterior knee) for improve range of motion in knee arthroscopy assisted anterior cruciate ligament reconstruction

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230125005
Enrollment
30
Registered
2023-01-25
Start date
2020-10-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

previous opioid use IPACK, Adductor canal block, knee arthroscopy assisted anterior cruciate ligament reconstruction, postoperative range of motion, Postoperative analgesia.

Interventions

Anterior cruciate ligament reconstruction was performed by single well-experienced surgeon via arthroscopy assisted procedure and graft selected with Hamstring Autograft. after finish surgery, patient
Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery
Adductor canal block ,Adductor canal block with IPACK

Sponsors

police general hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients who were diagnosed with anterior cruciate ligament tear of knee and scheduled for knee arthroscopy assisted anterior cruciate ligament reconstruction

Exclusion criteria

Exclusion criteria: 1) drug allergy for researched regimen 2) psychologic problem3) who are not command for collected data 4) renal function defect and Creatinine clearance < 50 ml/min 5) who could not do physical therapy 6) chronic pain 7) opioid addict or opioid dependence 8) multiple ligament injury of knee 9) inadequate control analgesia

Design outcomes

Primary

MeasureTime frame
Range of motion 2 days degree of knee flexion and extension

Secondary

MeasureTime frame
postoperative pain 2 days visual analogue scale (VAS) ,opioid consumption 2 days amount of dose (mg)

Countries

Thailand

Contacts

Public ContactNatthadech Thongmun

police hospital

doctorbenz2009@hotmail.com0910964654

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026