ClinicalTrials.Veeva

Menu

Regional Anesthesia in Hip Arthroscopy

University of Missouri (MU) logo

University of Missouri (MU)

Status

Withdrawn

Conditions

Femoroacetabular Impingement

Treatments

Drug: regional anesthesia placebo
Drug: regional anesthesia bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT02674113
1211908

Details and patient eligibility

About

The purpose of this research is to determine differences in outcomes in patients who receive regional anesthesia (a fascia iliaca block) versus placebo prior to undergoing hip arthroscopy with labral repair and/or debridement and osteoplasty for hip impingement.

Full description

Methods: After informed consent is obtained at a routine/pre-surgical clinic visit, all patients who meet eligibility criteria will undergo randomization into one of two groups. These groups are 1) to receive regional anesthesia (a single shot fascia iliaca block using bupivacaine) prior to hip arthroscopy, or 2) undergo a subcutaneous injection procedure using a normal saline placebo (0.9% sodium chloride in water) instead of bupivacaine. Intra-operatively, both groups will receive general anesthesia and local anesthesia (lidocaine and bupivacaine in the peripheral compartment).

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patient undergoing primary hip arthroscopy with labral repair and osteoplasty for hip impingement
  • Age 18-45 years old
  • Not pregnant
  • No history of neuropathic pain
  • No radiographic signs of osteoarthritis of the operative hip (Tönnisgrade 1)
  • Willing and able to comply with post-operative hip arthroscopy protocol
  • No documented allergy to anesthetic agents
  • Able to attend follow up appointments

Exclusion criteria

  • Allergy to regional anesthetic
  • Age <18 or >45 years
  • Pregnant females
  • History of neuropathic pain
  • Radiographic signs of osteoarthritis (Tönnis grade 2)
  • Unable to speak/understand English
  • Currently imprisoned
  • Unwilling/unable to provide consent

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

0 participants in 2 patient groups, including a placebo group

regional anesthesia bupivacaine
Active Comparator group
Description:
regional anesthesia (a single shot fascia iliaca block using bupivacaine) prior to hip arthroscopy
Treatment:
Drug: regional anesthesia bupivacaine
regional anesthesia placebo
Placebo Comparator group
Description:
subcutaneous injection procedure placebo (0.9% sodium chloride in water)
Treatment:
Drug: regional anesthesia placebo

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems