Comparision of headache in Spinal Anaesthesia in Cesarean section using different type of Spinal needles.
Phase 3
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2023/12/060449
- Lead Sponsor
- Vanaroja
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Female patient belonging to ASA1 and ASA2 posted for Elective Cesarean section.
Exclusion Criteria
1.Emergency Cesarean section
2.Patients with comorbidities and belonging to ASA3 and ASA4
3.Patients who are allergic to Local Anaesthesia and Adjuvants
4.Patient refusal to study
5.Underlying Severe Cardiac Pulmonary Compromise
6.Morbid obesity BMI >35
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the incidence and Severity of Post Dural Puncture Headache in terms of Numerical Analogue Scale[NAS]Timepoint: To determine the incidence and Severity of Post Dural Puncture Headache in terms of Numerical Analogue Scale[NAS] post operatively for each hour till first 48 hours
- Secondary Outcome Measures
Name Time Method To evaluate the incidence of Spinal needle induced Failed Spinal Anaesthesia <br/ ><br>To evaluate the incidence of other side effectsTimepoint: Intra operative period at baseline till the spinal anaesthesia achieved