comparing the effectiveness of different doses of norepinephrine immediately after giving spinal anaesthesia to prevent fall in blood pressure during caesarean section.
Completed
- Conditions
- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium,
- Registration Number
- CTRI/2020/04/024801
- Lead Sponsor
- Kasturba medical college
- Brief Summary
Comparison of efficacy of two different bolus doses of norepinephrine as prophylactic to prevent postspinal hypotension during elective caesarean section.
This study aims to compare the efficacy of two different bolus dosages of norepinephrine in effectively reducing the incidence of post spinal hypotension during elective caesarean section thereby improves maternal and fetal outcomes.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 84
Inclusion Criteria
- 1.Pregnant females undergoing elective caesarean section under spinal anaesthesia.
- 2.Full term pregnancy.
- 3.Singleton pregnancy.
- 4.BP range 90-140 mmHg 5.ASA physical status II 6.Age 18 years and older.
- 7.Weight between 50 and 100 kg.
- 8.Height between 150 and 170 cm.
Exclusion Criteria
- Patient refusal.
- Hypertension, cardiovascular or cerebrovascular disease.
- Fetal abnormalities.
- Diabetes (excluding gestational diabetes).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Success of prophylactic iv bolus of norepinephrine to maintain SBP at or above 80% of baseline from induction to delivery of foetus
- Secondary Outcome Measures
Name Time Method 1.Hypertension 2.Bradycardia
Trial Locations
- Locations (1)
Kasturba Medical College,Wenlock Government Hospital,Mangalore
🇮🇳Kannada, KARNATAKA, India
Kasturba Medical College,Wenlock Government Hospital,Mangalore🇮🇳Kannada, KARNATAKA, IndiaDr Garapati PranathiPrincipal investigator9666740160pranathi.garapati@gmail.com