NCT07644923

Postoperative Non-Opioid Pain Management Utilizing Local Anesthetics Coupled With Modulated Coagulation

Not Yet Recruiting
PHASE4Ages 18+InterventionalSupportive care
NYU Langone Health
~40 participants
Updated 2026-06-12 on ClinicalTrials.gov
What's tested:BupivacaineLidocaineThrombinTranexamic acidAminocaproic acid

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Pre-Operative Pain
Measured over Baseline (Day of Surgery)
+1 more outcome measured
Postoperative Pain
1 sites across 1 states
New York1
  • David Chiu, MD · PRINCIPAL_INVESTIGATOR · NYU Langone Health

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Eligibility criteria

Inclusion

Age 18 or older
Any patient undergoing elective hand surgery

Exclusion

Any patient with a traumatic or infected open wound (only surgically created wounds will be included)
History of chronic pain
History of narcotic addiction
History of recreational drug dependency
History of psychiatric pathology
Allergy or hypersensitivity to local anesthetics, recombinant human thrombin or tranexamic acid
History of coagulopathy or active thromboembolic disease
Any patient receiving a supra/infraclavicular block for anesthesia
Pregnancy
Hypersensitivity to hamster proteins
History of seizures
Significant renal impairment (chronic kidney disease stage 3 or greater)
History of retinal vascular disease or history of unexplained visual symptoms
Active upper urinary tract bleeding
History of known hypercoagulable disorder, prior thromboembolic events, or active clotting disorders
History of severe hepatic dysfunction (active hepatitis or steatohepatitis, hepatic fibrosis considered cirrhosis)
  • Pre-Operative PainBaseline (Day of Surgery)

    Pain rated on a scale from 0 (no pain) to 10 (highest level of pain ever experienced).

  • Post-Operative PainUp to Day 14 Post-Operative

    Pain rated on a scale from 0 (no pain) to 10 (highest level of pain ever experienced).