A study to know the effect of instillation of local anesthetic agent ,bupivacaine in abdomen for reliefof pain after cesarean sectio
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Primi gravida,of ASA grade 1 or2,aged between20 to 40 years, posted for planned or emergency cesarean section under spinal anesthesia
- Registration Number
- CTRI/2017/01/007679
- Lead Sponsor
- Government medical college surat
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
1.Primigravida posted for planned or emergency cesarean section under spinal anesthesia.
2.Patient who comes under ASA class 1 & 2 and age having between 20 yrs to 40 yrs.
Exclusion Criteria
1.Patient having previous abdominal surgery.
2.patient giving negative consent for this procedure.
3.patient allergic to bupivacaine.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO evaluate the duration of analgesia by bupivacaine (0.25%) instillation plus infiltration after cesarean section. <br/ ><br>2.Total requirement of other analgesic agent in 24 hours after cesarean section.Timepoint: Time when patient first ask for analgesic agent. <br/ ><br>24 hours after giving spinal anesthesia.
- Secondary Outcome Measures
Name Time Method 1.To study the side effect which may occurs following instillation plus infiltration of bupivacaine (0.25%). <br/ ><br>2.To evaluate the patient satisfaction for pain relief after cesarean section.Timepoint: during 24 hours after spinal anesthesia