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Comparison of vasopressors for treatment of hypotension during cesarean section.

Phase 4
Conditions
Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
Registration Number
CTRI/2023/08/056070
Lead Sponsor
TRIHMS Naharlagun
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Age group of 18 â?? 35 years

2.ASA II patients with full term pregnancy

3.Elective LSCS

4.Parturient giving informed written consent.

Exclusion Criteria

1. Known hypertensive patients, patients on anti-

hypertensive drugs & uncontrolled PIH

2. Multiple Gestations

3. Obese ( > 90 kg) or BMI >30 kg/m2

4. Short stature ( < 140 cm)

5. Haemoglobin < 9gm/dl

6. Patients with spinal deformity or puncture site infection

7. Known hypersensitivity to any of the 3 drugs

8. Patients with bleeding diathesis or coagulopathy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Which one is a better vasopresser in LSCS under spinal anaesthesiaTimepoint: Sample size in each arm is 40 . Total sample size of 3 arms is 120.
Secondary Outcome Measures
NameTimeMethod
Any side effect of drugsTimepoint: Any side effect of drugs
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