← Back to Search

Local Anesthetic

Erector spinae block for Hip Dysplasia

N/A

Waitlist Available

Led By Benjamin Coobs, MD

Research Sponsored by Carilion Clinic

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be younger than 65 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 1 year post-operatively

Awards & highlights

Study Summary

This trial will test if a preoperative erector spinae block can help with pain relief during arthroscopic hip surgery.

Eligible Conditions

Hip Dysplasia
Postoperative Pain

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 1 year post-operatively

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~1 year post-operatively

This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year post-operatively for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Opioids

Post Anesthesia Care Unit Pain

Secondary outcome measures

Hip disability and Osteoarthritis Outcome Score

Opioids

Outpatient Visual Analog Scale scores

+2 more

Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: StudyExperimental Treatment2 Interventions

Will receive an erector spinae block prior to surgery using 30-45 mL of 0.25 bupivacaine w/ epinephrine and 5 mL of dexmedetomidine. Will be administered 30 mL of 0.5% marcaine w/ epinephrine as a local block at the surgical site at the conclusion of the procedure.

Group II: ControlActive Control1 Intervention

Will not receive erector spinae block. Will be administered 30 mL of 0.5% Marcaine w/ epinephrine as a local block at the surgical site at the conclusion of the procedure.

Treatment

First Studied

Drug Approval Stage

How many patients have taken this drug

Erector spinae block

2022

N/A

~300

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

Carilion ClinicLead Sponsor

70 Previous Clinical Trials

12,595 Total Patients Enrolled

Benjamin Coobs, MDPrincipal InvestigatorCarilion Clinic Ortho Surgeon

Frequently Asked Questions

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

What aims does this research endeavor seek to accomplish?

"This clinical trial investigates Post Anesthesia Care Unit Pain over a 6 hour period post-operatively. Secondary measurements include Patient Reported Outcomes Measurement Information System Score, Range of Motion (Hip Flexion 0-110 degrees; Internal Rotation -5 – 25 degrees; External Rotation 0-60 degrees), and the Hip Disability and Osteoarthritis Outcome Score."

Answered by AI

To what demographic is participation in this trial open?

"The scope of this trial requires 120 individuals between 13 and 50 years old, with postoperative pain. Furthermore, they must possess the capacity to give their consent or assent for themselves before joining the study."

Answered by AI

Is the age of admittance for this experimental initiative limited to individuals aged 55 and above?

"According to the parameters of this trial, suitable patients must be between 13 and 50 years old. Conversely, there are 75 studies available for those younger than 18 and 395 trials open to seniors aged 65 or older."

Answered by AI

Does this clinical trial have any vacancies at present?

"Confirmed. Clinicaltrials.gov confirms that this trial is no longer seeking enrolment; the study was first posted on July 1 2021, and last updated June 4th 2021. Although this particular research has closed its recruitment process, there are 516 other trials recruiting participants at present time."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Evaluating the Efficacy of Erector Spinae Block in Routine Hip Arthroscopy

2021. "Evaluating the Efficacy of Erector Spinae Block in Routine Hip Arthroscopy". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04917510.