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
This trial does not accept healthy volunteersQualifiers
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 population
Patients aged 18-80 years, male and female, classified as ASA physical status I-III, and scheduled for elective lower abdominal surgery.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
spinal anaesthesia
Procedure/SurgeryPatients who will undergo surgery required spinal anaesthesia
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Paraspinal mass measurement with ultrasound.
Ultrasonographic measurement of paraspinal muscle thickness (cm) and its association with duration of spinal block will be investigated.
Time frame
Pre-operativeSecondary outcomes
1
The spread of the spinal block
The speed of the sensational block will be measured after spinal anaesthesia performed. Time(minute) will be recorded when T10 level sensational block is achieved.
Time frame
Perioperative/PeriproceduralSponsors and contacts
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Source ClinicalTrials.gov