Children With Fracture Femur Clinical Trial
Official title:
Effects of Dexmedetomidine Addition to Bupivacaine on the Quality of Fascia Iliaca Compartment Block (FICB) in Children Undergoing Femur Fracture Surgery
Verified date | March 2015 |
Source | Mansoura University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Egypt: Ministry of Higher Education |
Study type | Interventional |
Fractures of the shaft of femur (FSF) are common in children, especially isolated fractures
of the mid-third of the femur which are intensely painful. The pain of the fracture is
thought to originate from the femoral shaft periosteum and muscle spasm from the quadriceps
mechanism. Fascia iliaca compartment block FIC is easy and simple technique, there is no
need for high-skill or expensive equipments. It has higher success rate in more than 90%of
the children thigh procedures.
Potentially dexmedetomidine has become an alternative to clonidine, it is a highly selective
α2 agonist having about an 8-10 times affinity for α2 adrenergic receptors than clonidine
and much less α1 effects, which is responsible for the hypnotic and analgesic effects.
Perinural dexmedetomidine in combination with bupivacaine or ropivacaine enhance sensory and
motor block without neurotoxicity in experimental studies.It has been reported to improve
the quality of intrathecal, Epidural, and caudal anesthesia in children. Also, it is safe
and effective in IV regional anesthetic and axillary block in adult. No study-up to the date
-has been carried to evaluate its effect on the character of fascia iliaca compartment
blocks as adjuvant to bupivacaine. The objectives of this study were designed to detect the
effects of addition dexmedetomidine (Precedex- Abbot) as adjuvant to bupivacaine for fascia
iliaca block on the quality of postoperative analgesia and also to determine its effects on
the hemodynamics, recovery behaviors, sedation and possible side effects in children
undergoing thigh surgeries (fracture femur).
Status | Completed |
Enrollment | 28 |
Est. completion date | May 2012 |
Est. primary completion date | March 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 2 Years to 6 Years |
Eligibility |
Inclusion Criteria: - Children 2-6 years - American Society of Anesthesiologist physical class I and II - Fracture femur surgery Exclusion Criteria: - known allergy to the study drugs - suspected coagulopathy - infection at the site of the block - neurological diseases - history of developmental delay |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Egypt | Mansoura University Hospitals | Mansoura | DK |
Lead Sponsor | Collaborator |
---|---|
Mansoura University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Postoperative pain scores | Postoperative using the Objective Pain Scale (children <6 yr) which described by Hannallah et al. | every 4 hours after surgery | Yes |
Secondary | Vital signs | Heart rate, mean arterial pressure and oxygen saturation | before surgery, and every 20 min during surgery, and each 6 hours after surgery | Yes |
Secondary | Intraoperative hypotension | for 24 hours after surgery | Yes | |
Secondary | Intraoperative bradycardia | for 24 hours after surgery | Yes | |
Secondary | Postoperative sedation | Sedation score was assessed using Ramsay's sedation | every 4 hours after surgery | Yes |