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Popliteal Plexus Block for Postoperative Pain After ACL Reconstruction

The Effect of the Popliteal Plexus Block on Postoperative Pain After Reconstruction of the Anterior Cruciate Ligament

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03130049
Enrollment
15
Registered
2017-04-26
Start date
2017-09-27
Completion date
2017-12-04
Last updated
2018-01-23

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

Conditions

Anterior Cruciate Ligament Injury, Postoperative Pain

Keywords

Peripheral nerve block, Ultrasound

Brief summary

The study aims to investigate the effect of the popliteal plexus block (PPB) on postoperative pain in patients undergoing anterior cruciate ligament (ACL) reconstruction.

Detailed description

Postoperative pain following ACL reconstruction can be alleviated with an ultrasound-guided femoral triangle block (FTB). However, it is the investigators' observation that 10-20 % of the patients still complain of intense pain localized in the center of the knee. Cadaver dissection studies have shown that an injection into the distal part of the adductor canal will spread to the popliteal fossa, and one dissection study showed consistent spread to the popliteal plexus. The study team hypothesized that a PPB will reduce the postoperative pain, when it is used as a supplement to the FTB in patients undergoing ACL reconstruction.

Interventions

10 mL Marcain-adrenalin 5 mg/mL + 5 microgram/mL. Ultrasound-guided injection into the distal part of the adductor canal

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Pilot study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing ACL reconstruction on one of the two trial sites * Age ≥ 18 * American Society of Anesthesiologists (ASA) status I-III * Informed consent

Exclusion criteria

* Patients unable to cooperate * Patients not able to speak Danish or with other communication problems * Pregnancy * Contraindication towards any medical product used in the study * Preoperatively reduced sensation on the medial and lateral part of the lower leg * Patients with diabetes requiring medical treatment * Preoperative intake of opioids (dosed \> once daily) * ACL revision

Design outcomes

Primary

MeasureTime frameDescription
The effect of the popliteal plexus block (PPB)Pain scores (NRS): 15, 30, 45 and 60 minutes after PPBEvaluated as the percentage of patients with postoperative pain NRS \>3, dropping in pain score to NRS ≤ 3 after the PPB

Secondary

MeasureTime frameDescription
Percentage of patients with central knee painPain scores: 15, 30, 45 and 60 minutes after arrival at the post anesthesia care unit (PACU)The percentage of patients with FTB reporting pain (NRS \>3) localized in the center of the knee in the observation period
Onset time for PPBPain scores (NRS): 15, 30, 45 and 60 minutes after PPBTime from withdrawal of the needle until patient reports NRS ≤ 3
The effect of the PPB on cutaneous sensationBaseline, 30 and 60 minutes after PPBTested on the lateral part of the lower leg (pinprick test)
The effect of the PPB on muscle strengthBaseline, 60 minutes after PPBDorsal flexion and plantar flexion in the ankle joint, measured with a handheld dynamometer)

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026