NCT Number: NCT02804542
Fascia Iliaca Blocks and Pre-operative Opioid Requirements in Hip Fracture Patients
The purpose of this study is to determine if non-continuous local anesthetic fascia iliaca blocks performed in the emergency department are effective for preoperative analgesia in hip fracture patients. Investigators hypothesize that patients with these blocks will have lower opioid requirements than patients in a historical group in whom blocks were not performed.
Looking for future studies?
Notify MeKey information
Conditions
Age range
65 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- low energy femoral neck and pertrochanteric-type hip fractures
- age 65+
- intact cognition upon admission and ability to provide written informed consent
Exclusion criteria
- pathologic fractures (tumor)
- high energy fractures
- concomitant fractures besides hip fractures
- chronic home opioid exposure prior to hospitalization
- moderate to severe dementia
- pre-fracture hospitalization
- time from arrival to block >6 hours
- time from arrival to OR <6 hours or >48 hours
Treatment and study plan
Retrospective review
OtherPrimary outcomes
-
Total Pre-op IV Morphine Equivalents (TIVME)
Time frame: From Date of admission until date of surgery, approximately 48 hours
IV morphine equivalent dosing pre-operatively
Secondary outcomes
-
Mean Pre-op Pain Score
Time frame: From Date of admission until date of surgery, approximately 48 hours
Mean patient-reported pain score
-
Length of Hospital Stay (LOS)
Time frame: Through study completion, approximately 5 days
Sponsors and collaborators
Lead sponsor
Corewell Health West
Other
Collaborators
- Grand Rapids Medical Education Partners
Registry information
Official study title
Pre-operative Fascia Iliaca Blocks and Opioid Requirements in Hip Fracture Patients
Important dates
- Study start
- 2016
- Primary completion
- 2019
- Study completion
- 2019
- First posted
- Jun 17, 2016
- Registry last updated
- Sep 22, 2023
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.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Comparison of the Efficacy of Ultrasound-guided Supra-inguinal Fascia Iliaca and Lumbar Erector Spina Plan Block in Hip Fractures
NCT07639762
Agnosia, Femoral Fractures
Istanbul, Sancaktepe, Turkey (Türkiye)
View Trial DetailsImplementation of the MOX Activity Monitor in Hospitalized Geriatric Rehabilitation
NCT07124247
Brain Diseases, Cardiovascular Diseases
Pellenberg, Belgium
View Trial DetailsFascia Iliaca vs Femoral Nerve Block in Hip Fracture Patients
NCT07597317
Femoral Fractures, Femoral Nerve
Lahore, Punjab Province, Pakistan
View Trial DetailsEffect of PENG Block on Postoperative Tramadol Consumption in Partial Hip Prosthesis Surgery
NCT07534137
Femoral Fractures, Fractures, Bone
Gaziantep, Turkey (Türkiye)
View Trial Details