Caudal Block,Saddle Block, Anorectal Surgery
Anorectal Disorder
About this trial
This is an interventional supportive care trial for Anorectal Disorder focused on measuring caudal block, saddle block
Eligibility Criteria
Inclusion Criteria:
- 18-60 years old patients
- ASA 1-2 patients
- Patients who will undergo anorectal surgery
Exclusion Criteria:
- Having known hypersensitivity to amide type local anesthetics
- Patients with contraindications to central block (caudal, saddleblock): use of anticoagulant medication, local infection in the intervention site, increased intracranial pressure, severe aortic and / or mitral valve stenosis, ischemic hypertrophic subaortic stenosis,
- Patients who do not accept regional anesthesia
Sites / Locations
- Derince Eğitim Ve Araştırma Hastanesi
- Şimşek
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Caudal Block
Saddle Block
For the caudal block, sacral horns are palpated and sacral hiatus and epidural area will be determined at S4-S5 level through ultrasonography. The 20 G adult caudal needle will then be placed to the caudal epidural space and 25 mL bupivacaine at a concentration of 0.5% will be applied in the prone Jack-Knife position with resistance loss.
In the saddle block group hyperbaric bupivacaine at a dose of 7 mg will be given to the intrathecal space after a 25 G quincke spinal needle is inserted with ultrasonography guidance between L4-L5 vertebral disc and clear cerebrospinal fluid is seen. The patient will be placed in sitting position for 5 minutes.