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Clinical Trials in Turkey / NCT07638280
Recruiting Observational

Non-Pharmacological Factors on Spinal Block Duration

NCT07638280 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-06-16
Last updated
2026-06-23

Condition(s) studied

Paraspinal Muscle Mass and Spinal Anaesthesia

Investigational drug(s) / intervention(s)

spinal anaesthesia

spinal anaesthesia: Patients who will undergo surgery required spinal anaesthesia

Study summary

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

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18-80 years * ASA physical status I-III * Patients scheduled for elective lower abdominal surgery. Exclusion Criteria: * Patient refusal to participate * Coagulopathy * Use of medications or substances known to impair coagulation * Pregnancy, sepsis * Shock * Severe aortic or mitral regurgitation * Peripheral vascular disease * Increased intracranial pressure * Mental disorders * Spinal column deformity * History of previous spinal surgery.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Taksim Training and Research Hospital Istanbul Turkey (Türkiye) Recruiting

More Taksim Egitim ve Arastirma Hastanesi trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07638280 on ClinicalTrials.gov ↗ ← All trials in Turkey