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NCT06575010

Exparel v Dexamethasone in RCR

UNKNOWN
PHASE4Ages 18+InterventionalTreatment
Rothman Institute Orthopaedics
~126 participants
Updated 2024-08-28 on ClinicalTrials.gov
What's tested:Liposomal bupivacaineBupivacaine Hcl 0.5% InjDexamethasone

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Postoperative narcotic medication use
Measured over 14 days
+1 more outcome measured

Conditions

Rotator Cuff Tears
Postoperative Pain

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NCT06575010

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.

  • Rothman Orthopaedic Institute

    Philadelphia, Pennsylvaniano site contact published

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

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

Participants having a primary rotator cuff repair
Age 18 and older
English speaking
Ability to complete surveys by phone or in person
Ability to provide informed consent

Exclusion

Revision rotator cuff repair (RCR) cases
Participants having an open RCR
Allergies and/or medical contra-indications to study medications
Non-English speakers
Participants who are pregnant, plan to become pregnant and do not utilize adequate contraceptive means, or are currently breastfeeding (all patients who have the potential to be pregnant are administered a urine beta-HCG pregnancy test, with suspected false-positive or equivocal urine pregnancy tests followed by a more specific serum pregnancy test)
Rotator cuff repair needing Graft Augmentation
Known alcohol or narcotic abuse history
Existing contract with a pain specialist due to underlying preoperative pain syndrome
Preoperative opioid use within the 3 months prior to surgery

What this trial measures

  • Postoperative narcotic medication use14 days

    Participants will be asked to record the amount of medication they take to control pain after surgery

  • Postoperative pain levels14 days

    This will be measured by providing participants the visual analog scale (VAS) questionnaire as well as a postoperative pain recording diary to complete after surgery