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comparing the efficacy of inj. Bupivaccaine and inj. ropivaccaine as analgesia in cesarean sectio

Phase 4
Conditions
Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Registration Number
CTRI/2019/07/020098
Lead Sponsor
Department of Pharamcology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Informed written consent for participation in study.

2. Age: 20 to 35 years

3. Antenatal female patients scheduled for lower segment cesarean scetion.

4. Primi patients undergoing LSCS d/t CPD, Diabetes, Placenta Previa.

5. Singleton pregnancy

6. ASA physical status 1 and 2

Exclusion Criteria

1. Patient refusing consent.

2. Multiple pregnancy

3. Mutipara

4. Neuropsychiatric disorder

5. Patient having post partum psychosis.

6. Allergy or hypersensitivity to local anesthetic or NSAIDS.

7. Anemia

8. Patient on any form of analgesics therapy.

9. Patient on ECG showing QT prolongtion.

10. ASA pysical status 3 and 4.

11. Contraindication to spinal anesthesia

- Local infection or sepsis at site of Lumbar Puncture.

- Bleeding disorders, thrombocytopenia

- Space occupying lesons of the brain.

- Anatomical disorder of spine

- Hypovolemia e.g. following massive hemorrhage

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
-Visual Analogue Scale (VAS) <br/ ><br>-Patients satisfaction score <br/ ><br>-Surgeons satisfaction score <br/ ><br>-Total dose and frequency of rescue anlgesia.Timepoint: -30 min, 2,4,6,12,16,20,24
Secondary Outcome Measures
NameTimeMethod
Effect on hemodynamic parmeters like heart rate, mean arterial pressure, oxygen saturation <br/ ><br>- side effects and comlications if anyTimepoint: 30 min, 2,4,6,12,16,20,24
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