Non-Pharmacological Factors on Spinal Block Duration
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorTaksim Egitim ve Arastirma Hastanesi
About this trial
The aim of this study is to evaluate the effects of non-pharmacological factors-such as age, sex, body mass index, paraspinal muscle mass, vertebral canal anatomy, patient positioning, and injection technique-on the duration of sensory and motor block in patients undergoing spinal anesthesia, and to investigate the potential relationships between these factors and block duration.
Eligibility criteria
Qualifiers
Patients aged 18-80 years
ASA physical status I-III
Patients scheduled for elective lower abdominal surgery.
Disqualifiers
Patient refusal to participate
Coagulopathy
Use of medications or substances known to impair coagulation
Pregnancy, sepsis
Trial design
Treatments tested in this trial
- spinal anaesthesia
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov