Pain after Ceserean section- to compare Paracetamol and Dexamethasone intravenously.

Not Applicable

• Conditions: Health Condition 1: O748- Other complications of anesthesiaduring labor and delivery

• Registration Number: CTRI/2021/07/034872
• Lead Sponsor: Dr Snigdha Bellapukonda

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

After approval of our Institutional Ethical Committee and obtaining informed consent. American Society Anesthesiologists (ASA) II pregnant patients posted for elective Caesarean section of age 18-35 years will be enrolled in the study with height >140cm.

Exclusion Criteria

Pregnant patients with

I. Diabetes mellitus

II. Chorioamniotis

III. Preeclampsia

IV. Pregnant women having contraindication to spinal anaesthesia, those who have accompanying, placenta praevia, and twin pregnancy, those whose weight will be < 50 kg or > 100 kg, height < 140 cms those with cardiopulmonary disease, cerebrovascular diseases, autonomic neuropathy, spinal deformities, other neurological diseases, infections in the lumbar area, coagulation abnormalities, hypovolemia due to any cause and systolic blood pressure (SBP) < 100 mmHg, fetal distress will be excluded from the study. Patients with placental complications (placenta praevia or placental abruption), cord complications (nuchal cord or cord prolapse), fetal malformations, premature deliveries. All other patients requiring emergency cesarean sections. Patients already on chronic steroid use.

V. All cesarean sections planned for or converted to General Anesthesia.

Study & Design

• Study Type: Interventional
• Study Design: Not specified