CompletedPhase 4

Hip Scope Fascia-iliaca (FI) Block Study

United States84 participantsStarted 2015-04

Plain-language summary

Patients undergoing a hip scope procedure will be recruited for this study. They will be randomized to either receive a nerve block or no nerve block (pain medicine only). Pain levels and clinical outcomes will be assessed through 3 months post-operatively.

Who can participate

Age range18 Years – 65 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Scheduled for outpatient hip arthroscopy * American Society of Anesthesiologists (ASA) 1-3 Exclusion Criteria: * Prior surgery on ipsilateral hip * ASA 4-6 * Chronic narcotic usage over 6 months or more than the equivalent of 20mg of morphine per day * Current or prior placement of a spinal cord stimulator or intrathecal pump for pain control purposes * Allergy to amide local anesthetics * Contraindication to regional anesthesia * BMI \> 40 * Females who are pregnant or plan to get pregnant during the course of the study

What they're measuring

Visual Analog Scale

Timeframe: 3 Months

Trial details

NCT IDNCT02365961

SponsorThe Hawkins Foundation

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-06

Results submitted2018-10-31

View on ClinicalTrials.gov More Hip Dysplasia trials