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CMP for Postoperative Pain

N/A
Waitlist Available
Research Sponsored by Loyola University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights

Summary

This trial is testing a new way to do a nerve block that may minimize the amount of pain medication needed post-operatively.

Eligible Conditions
  • Postoperative Pain
  • Hip Replacement

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 hours for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Measurement of opioid use
Secondary outcome measures
Measurement of the pain control

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: CMPExperimental Treatment1 Intervention
Cluneal nerve Block 0.25% bupivacaine 20ml Pericapsular Nerve group block 0.25% Bupivacaine 20ml Lateral femoral cutaneous Block 0.25% bupivacaine 10ml
Group II: Fascia iliacaActive Control1 Intervention
Fascia iliaca block suprainguinal technique 0.25% bupivacaine 50ml
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CMP
2008
N/A
~20

Find a Location

Who is running the clinical trial?

Loyola UniversityLead Sponsor
156 Previous Clinical Trials
31,061 Total Patients Enrolled
~8 spots leftby Jul 2025
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