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Local Anesthetic

Exparel Administration for Hip Fracture (HEAT Trial)

Phase 4
Waitlist Available
Led By Daniel Komlos, MD, PhD
Research Sponsored by Maimonides Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 and 48 hours after surgery
Awards & highlights

HEAT Trial Summary

This trial will study whether Liposomal Bupivacaine (Exparel) is effective in reducing pain for hip fracture patients undergoing hip hemiarthroplasty for femoral neck fractures.

Eligible Conditions
  • Hip Hemiarthroplasty
  • Femoral Neck Fracture

HEAT Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~48 hours after surgery
This trial's timeline: 3 weeks for screening, Varies for treatment, and 48 hours after surgery for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Post-operative Pain
Secondary outcome measures
Delirium Scale Measurements
Length of Stay
Postoperative Total Morphine Equivalent
+1 more

HEAT Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Bupivacaine liposomeExperimental Treatment1 Intervention
This arm will receive Exparel along with Bupivacaine
Group II: SalinePlacebo Group1 Intervention
This arm will receive Saline along with Bupivacaine
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Bupivacaine
FDA approved

Find a Location

Who is running the clinical trial?

Maimonides Medical CenterLead Sponsor
69 Previous Clinical Trials
15,245 Total Patients Enrolled
Daniel Komlos, MD, PhDPrincipal InvestigatorMaimonides Medical Center
Kevin Kang, MDStudy DirectorMaimonides Medical Center

Media Library

Bupivacaine Liposome (Local Anesthetic) Clinical Trial Eligibility Overview. Trial Name: NCT03502018 — Phase 4
Hip Hemiarthroplasty Research Study Groups: Saline, Bupivacaine liposome
Hip Hemiarthroplasty Clinical Trial 2023: Bupivacaine Liposome Highlights & Side Effects. Trial Name: NCT03502018 — Phase 4
Bupivacaine Liposome (Local Anesthetic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03502018 — Phase 4

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there other findings connected to the utilization of Bupivacaine liposome?

"As of now, 18 Phase 3 trials for Bupivacaine liposome are active and being conducted at a total of 109 locations. Most studies are located in Philadelphia, Pennsylvania; however 144 sites around the world have opened their doors to this study."

Answered by AI

What conditions is Bupivacaine liposome typically prescribed to alleviate?

"Bupivacaine liposome is the go-to treatment for pemphigus, but it has also been known to effectively tackle other conditions like acute nonspecific tenosynovitis, general anesthesia, and lupus erythematous."

Answered by AI

Is this venture currently recruiting participants?

"This research study is currently open for patient enrollment, as indicated on clinicaltrials.gov. Its first listing was made on March 1st 2018 and it was last updated on August 9th 2022."

Answered by AI

Has the United States Food and Drug Administration accepted Bupivacaine liposome as a viable medical treatment?

"We at Power have concluded that Bupivacaine liposome is a safe treatment, awarding it with a 3 out of 3 rating. This judgement was made as the medication has already received FDA approval and thus entered its fourth stage of clinical trial."

Answered by AI

How many individuals are accepted into this research endeavor?

"Affirmative. Clinicaltrials.gov exhibits that this experiment is open to recruitment and was first published on March 1st, 2018. The most recent update was August 9th, 2022 and the study requires 50 volunteers across a single medical site."

Answered by AI
~7 spots leftby Apr 2025