An Observational study to study the effect of anthropometric measurements and drug baricity on spinal aneasthesia
Not Applicable
- Conditions
- Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2020/01/022917
- Lead Sponsor
- Dr Umme Sarah
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1&2
Weight 50-100 kgs
Height 140-180cms
Elective surgeries
Exclusion Criteria
Patients hat rejected the study or spinal anaesthesia
Contraindications for spinal Anaesthesia
Present severe Cardiovascular disease
Prior spine and spinal canal surgeries
ASA more than 2
Emergency surgeries
Patients shorter than 145 and taller than 180cms
Known Allergy to Local anesthetic agent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method effect of baricity on the spread of drug, total level of spinal anaesthesia, time to reach maximum sensory blockadeTimepoint: Pin prick test will be done in the mid clavicular line at 5mins, 10mins, 20 mins, 30 mins after the drug is deposited
- Secondary Outcome Measures
Name Time Method ilTimepoint: Nil