Pain Management After ACL Surgery in Teens and Young Adults

This study is looking at how well a nerve block helps manage pain after surgery for a torn ACL (a knee ligament). Researchers want to see if using a single shot of Ropivacaine 0.2% Injectable Solution around the nerves before surgery can reduce pain and the need for strong pain medications (narcotics) for up to one week after surgery. You might be able to join if you are 13 to 21 years old and need ACL surgery using a specific type of graft. The study will measure your pain using different scales and questionnaires on days 1, 4, and 7 after your surgery. The goal is to enroll 160 participants.

Study design
This is a randomized controlled trial, meaning participants will be randomly assigned to receive the nerve block or not. It is single-blinded, so you won't know if you received the nerve block, but the doctors will. The study aims to enroll 160 participants.
What's involved
You will be approached before surgery to participate. Your pain levels will be measured using different scales and questionnaires on days 1, 4, and 7 after your surgery.
Compensation
Not stated in the trial record.
Follow-up
Your pain levels will be monitored for up to one week after surgery, specifically on postoperative days 1, 4, and 7.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06559137

Evaluation of Pain Management After Surgery When Using Nerve Blocks in the Pediatric Population

Not Yet Recruiting
PHASE2Ages 13–21InterventionalTreatment
Texas Scottish Rite Hospital for Children
~160 participants
Updated 2025-09-16 on ClinicalTrials.gov
What's tested:Ropivacaine 0.2% Injectable Solution

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Visual Analog Scale (VAS) Wong-Baker Face Pain Scale
Measured over Postoperative days 1, 4, and 7
+3 more outcomes measured
Anterior Cruciate Ligament (ACL) Tear
Sports Injuries in Children
Analgesia
Pain, Postoperative

NCT06559137

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Texas Scottish Rite Hospital for Children

    Frisco, Texasstudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Philip Wilson, MD · PRINCIPAL_INVESTIGATOR · Texas Scottish Rite Hospital for Children

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Eligibility criteria

Inclusion

Must be aged 13+ years at time of surgery
Must present with injury requiring an ACLR procedure with a Bone Patellar Tendon Bone or Quadriceps graft
Ability to provide assent, legally appointed representative available to provide informed consent

Exclusion

Patient \<13 years old
Requires fracture repair or another non-standardized surgery
Any ACLR that requires the use of a graft type other than Bone Patellar Tendon Bone or Quadriceps tendon
Any lower extremity procedure that is not primarily an ACLR
Patient pregnancy
Inability to provide assent or legally appointed representative to provide informed consent
Prior history of hypersensitivity to Ropivacaine or any local anesthesia
BMI ≥ 40
  • Visual Analog Scale (VAS) Wong-Baker Face Pain ScalePostoperative days 1, 4, and 7

    Scale with evocative faces from 0-10 (0 = No Pain, 10 = Worst Pain Possible) that assists children in communicating about their pain

  • Visual Analog Scale (VAS) 10-centimeter line 0-10 Numeric Pain Intensity ScalePostoperative days 1, 4, and 7

    Sliding scale from 0-10 (0 = No Pain, 10 = Pain as bad as it could possibly be) that enables a more accurate estimate of pain score

  • Scottish Rite for Children-developed pain questionnairePostoperative days 1, 4, and 7

    Institutional questionnaire that asks how many narcotic pills the patient has taken (0 - 12 pills), if their pain is controlled, treatments that lessens their pain, term that best describes their pain, how much their pain has interfered with daily tasks and overall mood, and sleep interference due to pain.

  • Pain Management Patient Satisfaction questionnairePostoperative day 7

    Questionnaire that asks how satisfied patients are with their pain treatment (0 = Not Satisfied, 10 = Extremely Satisfied), if they contacted their physician due to ineffective pain treatment, how helpful the information provided for pain treatment was (0 = Not Helpful, 10 = Extremely Helpful), and a free response section to explain why they were not satisfied with their pain treatment and if they have any additional comments or suggestions based on their pain treatment.