se of pain reducing spray for spinal needle puncture
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065761
- Lead Sponsor
- Dr Annu choudhary
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted for elective caesarean section under subarachnoid block.
Exclusion Criteria
1.Patient’s refusal to participate
2.Any allergy to local anesthetics
3.Coagulation disorders
4.Infection at the site of intervention
5.History of any underlying cardiac, renal dysfunction
•Viral marker status positive
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare maternal satisfaction for anaesthesia service at the end of surgery by 5 point likert scaleTimepoint: At the Post anesthesia Care Unit (0 hr)
- Secondary Outcome Measures
Name Time Method 1.Comparison of pain on spinal needle insertion <br/ ><br>2.Comparison of number of pricks required for administering spinal anaesthesia <br/ ><br>3.Investigate whether pain during puncture has an influence on choosing spinal anaesthesia again in the futureTimepoint: after injecting drug in subarachnoid space for spinal anaesthesia & at the end of surgery