To study the effect of different body parameters on the spread of subarachnoid block in elective lower segment cesarean section.
Not Applicable
- Registration Number
- CTRI/2023/03/051164
- Lead Sponsor
- Sapthagiri Institute of Medical Sciences and Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Partutrients willing to take part in the study
2. Term gestation parturient posted for elective LSCS under spinal anesthesia
3. ASA Grade 2
4. Age 18 to 35 years
Exclusion Criteria
1. Parturient undergoing general anesthesia
2. Any abnormalities of the spine
3. Local infection
4. Bleeding disorders
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms influence subarachnoid block spread in relation to BMI and vertebral column length during elective cesarean sections?
How does the hip-shoulder width ratio affect the efficacy and safety of subarachnoid block in patients with varying BMI categories undergoing lower segment cesarean sections?
Are there specific biomarkers that correlate with the spread of subarachnoid block in obstetric anesthesia for elective cesarean deliveries?
What adverse events are associated with subarachnoid block in patients with high BMI or abnormal vertebral column length during cesarean sections?
How do current subarachnoid block techniques compare to alternative spinal anesthesia approaches in terms of spread and outcomes for elective lower segment cesarean sections?