NCT06575010
Exparel v Dexamethasone in RCR
Enrolling by Invitation
PHASE4Ages 18+InterventionalTreatmentRothman Institute OrthopaedicsInvestigator-initiated
~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
Where it's being run
1 sites across 1 statesPennsylvania1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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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