Skip to content

Pain Control in Hip Arthroscopy: Comparing Lumbar Plexus Versus Peri-capsular Injection

Prospective, Single Blind Randomzied Controlled Trial Comparing Lumbar Plexus Peripheral Nerve Block Versus Peri-capsular Injection for Hip Arthroscopy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03244631
Enrollment
64
Registered
2017-08-09
Start date
2017-09-26
Completion date
2020-02-01
Last updated
2020-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nerve Block, Hip Arthroscopy

Brief summary

Comparison of lumbar plexus nerve block versus pericapsular injection for pain control during hip arthroscopy

Detailed description

The purpose of this study is to compare two different methods of pain control during and after hip arthroscopy surgery. It is not clear which of many different pain control methods are ideal to reduce pain for patients; consequently, the investigators are performing this study to compare the two main choices for pain control commonly used in order to identify if either is superior to the other.

Interventions

Peripheral nerve block

Injection around the area undergoing surgery

Sponsors

Washington Orthopaedics and Sports Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Prospective randomized

Eligibility

Sex/Gender
ALL
Age
25 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patient scheduled to undergo hip arthroscopy with Dr. Wolff 2. Patient age between 25 and 60 years of age.

Exclusion criteria

1. Patient has known allergy to ropivicaine or morphine. 2. Patient unable to speak/read English (No translators available in clinic site). 3. Pregnant female. 4. Patient has a pre-operative narcotic use for hip pain 5. Patient has pre-existing chronic pain disorder (i.e. fibromyalgia)

Design outcomes

Primary

MeasureTime frameDescription
Pain scoreAt the one hour point in the PACUCompare post-operative pain scores in the immediate post-operative period as defined by visual-analog pain scale at the time point of one hour spent in the post-anesthesia care unit (PACU).

Secondary

MeasureTime frameDescription
Morphine equivalentsAt the two hour point in the PACUCompare the total morphine equivalents of opioids provided in the PACU within the first two hours of time spent in the PACU
Time spent in PACUImmediately after surgeryCompare the overall time spent in the PACU as defined by time to arrival to time to discharge vitals.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026