A comparative study to determine total vasopressor requirement in elective caesarean section in Specified Conditio

Not Applicable

• Conditions: Health Condition 1: O- Medical and Surgical

• Registration Number: CTRI/2022/07/044277
• Lead Sponsor: Dr Yoganarasimha

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 2 August 2022

Recruitment & Eligibility

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

Inclusion Criteria

1. Patients willing to give informed consent.

2. ASA 2 patients.

3. Pregnant females at term.

4. With uncomplicated pregnancies.

5. Elective LSCS.

6. Height of the patient between 150 - 170 cms.

Exclusion Criteria

1. Unstable haemodynamic, cardiovascular insufficiency or fixed cardiac output states.

2. Hypertensive disorders of pregnancy, diabetes mellitus or other causes of peripheral neuropathy and autonomic dysfunction.

3. Pregnant ladies with foetal anomalies and twin gestation.

4. Known history of allergy to local anaesthetics or study drugs.

5. Patients with coagulation abnormalities, or on anticoagulants.

6.Features of soft tissues infection at the site of sub arachnoid block.

7. Chronic/essential hypertension, vasculitis/vascular disorder.

8. Contraindications to sub arachnoid block.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the vasopressor requirement in both the groupsTimepoint: 0 to 10 minutes after SAB and at 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes of surgery

Secondary Outcome Measures

Name	Time	Method
Overall Safety of the drugsTimepoint: 0 to 10 minutes after SAB and at 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 35 minutes, 40 minutes, 45 minutes, 50 minutes, 55 minutes, 60 minutes of surgery