Status:
COMPLETED
Evaluation of Caudal Block and Ilioinguinal-ilioohypogastric Nerve Block Efficacy with Perfusion Index (PI)
Lead Sponsor:
Bursa Yuksek Ihtisas Training and Research Hospital
Conditions:
Perfusion Index
Plethysmography
Eligibility:
All Genders
2-8 years
Phase:
NA
Brief Summary
The study is a prospective, randomised, controlled double-blind clinical trial. The primary aim was to evaluate the efficacy of caudal block and ilioinguinal-iliohypogastric nerve block with PI and PV...
Detailed Description
The study is a prospective, randomised, controlled double-blind clinical trial. The primary aim was to evaluate the efficacy of caudal block and ilioinguinal-iliohypogastric nerve block with PI and PV...
Eligibility Criteria
Inclusion
- 2-8 years old
- Elective Inguinal hernia operation
- ASA I-II patients
Exclusion
- \<2 years to be \>8 years old
- ASA III-IV patients
- Peripheral vascular disease
- Diabetes Mellitus patient
- Neuromuscular disease
- Bleeding disorder
- Infection in the area to be blocked
- Infection at the perfusion index probe adhesion site
- Bilateral inguinal hernia operation
- Inguinal hernia operation with circumcision
- Cases taken to emergency operation
- Mental retardation
- Not knowing Turkish
- Allergy to local anesthetics
- Refusal to participate in the research
Key Trial Info
Start Date :
January 18 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2024
Estimated Enrollment :
102 Patients enrolled
Trial Details
Trial ID
NCT06203743
Start Date
January 18 2024
End Date
June 1 2024
Last Update
February 19 2025
Active Locations (1)
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1
Bursa Yuksek Ihtisas Training and Research Hospital
Bursa, Bursa, Turkey (Türkiye)