Viewing Study NCT06249789



Ignite Creation Date: 2024-05-06 @ 8:04 PM
Last Modification Date: 2024-10-26 @ 3:20 PM
Study NCT ID: NCT06249789
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-02-08
First Post: 2024-01-25

Brief Title: Enhancing Recovery in Hip Fracture Surgeries
Sponsor: Hartford Hospital
Organization: Hartford Hospital

Study Overview

Official Title: Enhancing Recovery in Hip Fracture Surgeries
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to look at how two different types of anesthesia spinal and general affect participants with broken hips who are getting a special kind of pain block before surgery

Researchers will check

How quickly patients are ready for anesthesia
How long they stay in the recovery room after surgery
How much pain medicine they need during recovery
If they experience any confusion
If one group has complications in one of these anesthesia techniques

Participants in the study will be put into one of two groups by chance to see if theres a difference in their recovery
Detailed Description: This clinical trial aims to compare two common anesthesia techniques spinal and general anesthesia combined with a preoperative nerve block called the Fascia Iliaca Compartment Block FICB The objective is to understand how these methods affect patients undergoing hip fracture surgery

The main questions this study aims to answer are

Does the choice between spinal and general anesthesia influence how quickly patients recover from anesthesia
Does it affect how long patients stay in the Post-Anesthesia Care Unit PACU
Does it change the amount of opioid pain medication needed after surgery
Do the different anesthesia types impact the occurrence of postoperative delirium
Do they affect the length of the hospital stay after surgery
Do they lead to different rates of post-operative complications

Participants will

Receive either spinal anesthesia with Fascia Iliaca Compartment Block FICB Arm A or general anesthesia with Fascia Iliaca Compartment Block FICB Arm B
Undergo an ultrasound-guided FICB injection
Receive appropriate anesthesia and sedation during surgery
Be monitored for pain and provided with pain relief as needed

The studys broader objectives include enhancing patient safety and satisfaction reducing hospital readmission rates lowering healthcare costs and improving overall healthcare practices Although direct benefits to participants are not guaranteed the findings will inform better care for future patients with hip fractures

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: None