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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05705726
Other study ID # 524/2022
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 11, 2023
Est. completion date July 1, 2024

Study information

Verified date October 2023
Source Minia University
Contact hassan m. hetta, lecturer
Phone 1010901114
Email hassan.hetta@mu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Proximal femur fractures are one of the commonest fractures especially in the elderly population. Early surgical fixation is the best analgesic for associated pain. Spinal anesthesia has been favored by many anesthesiologists due to the simplicity of the technique, the better analgesic profile, and the lower incidence of complications like delirium and thromboembolic events. However, severe pain, encountered during positioning for spinal anesthesia, can complicate the technique and worsen the patient experience. the study aim to compare the analgesic effect of intravenous dexmedetomidine and fascia iliaca block preoperatively to assist positioning patients for performance of spinal anesthesia.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date July 1, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: 1. Aged 18-60 years. 2. Hip fractures 3. Both sexes. Exclusion Criteria: 1. Patient refusal 2. Allergy to local anesthetics 3. Bleeding diathesis or history of anticoagulant use. 4. impaired cognition or dementia 5. . Infection of the skin at the site of needle punctures area 6. multiple fractures 7. Any previous analgesic administration during the last 12 hours

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ultrasound guided facia iliaca block
Patient will received ultrasound guided fascia iliaca block by 20 ml Bupivacaine 0,25% .
Drug:
Intravenous drug
Patient will received intravenous injection of precedex 0.25mic/Kg and ketamine 0,2 mg/kg .

Locations

Country Name City State
Egypt Minia University Hospital Minya

Sponsors (1)

Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Behavioral pain scale 0 = calm, 1 = facial grimacing, 2 = moaning, 3 = screaming, and 4 = unable to proceed because of restlessness or agitation during spinal anesthesia
Secondary Quality of patient's position 0 = poor hip flexion, 1 = satisfactory hip flexion, 2 = good hip flexion, and 3 = optimal hip flexion before spinal anesthesia
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