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NCT04086914 Clinical Trial

Fascia Iliaca Compartment Blocks for Pain Control in Hip Fractures

Hip Fractures Clinical Trial

Official title:
Fascia Iliaca Compartment Blocks to Improve Preoperative Pain Control in Elderly Hip Fractures

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT04086914
Other study ID # 00090054
Secondary ID
Status Withdrawn
Phase Early Phase 1
First received
Last updated
Start date February 1, 2020
Est. completion date December 1, 2020

Study information
Verified date February 2020
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is comparing the use of a peripheral nerve block and standard opioid pain medications in pain control in hip fractures prior to surgery. A peripheral nerve block is a procedure that injects numbing medicine around a nerve to help decrease the pain, motion, and sensation around the painful site temporarily. The purpose of this study is to evaluate if peripheral nerve blocks are more effective for pain control than just standard opioid pain medication while decreasing the amount of side effects from opioid medication.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date December 1, 2020
Est. primary completion date November 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 100 Years
Eligibility Inclusion Criteria:

- Aged 50 or older, low energy hip fracture, acute hip fracture

Exclusion Criteria:

- On anticoagulants, hardware present near injection site, preexisting nerve injury.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Nerve Block
This group will receive a nerve block consisting of 20mL of 5mg/mL ropivicanine and 0.1mL of 10mg'mL dexamethasone.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Medical University of South Carolina

Outcome
Type Measure Description Time frame Safety issue
Primary Mean Baseline Pain score on Visual analogue scale at initial encounter pain is measured 1-10, 1 being the lowest and 10 being the highest 0-60 minutes
Primary Mean Change from baseline pain score on the visual analogue scale pain is measured 1-10, 1 being the lowest and 10 being the highest 3-8 hours after initial encounter
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