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Completed

NCT Number: NCT03244631

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

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

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Key information

Age range

25 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Washington Orthopedics and Sports Medicine

Chevy Chase, Maryland, 20815, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

lumbar plexus block

Procedure

Peripheral nerve block

Pericapsular injection

Procedure

Injection around the area undergoing surgery

Primary outcomes

  1. Pain score

    Time frame: At the one hour point in the PACU

    Compare 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 outcomes

  1. Morphine equivalents

    Time frame: At the two hour point in the PACU

    Compare the total morphine equivalents of opioids provided in the PACU within the first two hours of time spent in the PACU

  2. Time spent in PACU

    Time frame: Immediately after surgery

    Compare the overall time spent in the PACU as defined by time to arrival to time to discharge vitals.

Sponsors and collaborators

Lead sponsor

Washington Orthopaedics and Sports Medicine

Other

Registry information

Official study title

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

Important dates

Study start
2017
Primary completion
2018
Study completion
2020
First posted
Aug 9, 2017
Registry last updated
Feb 12, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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