A study to compare two different route of using Phenylephrine in order to prevent hypotension in pregnant patients
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2022/01/039516
- Lead Sponsor
- Dr Sankar Roy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients need emergency LUCS
2.Patients of ASA 1 and ASA 2.
3.Age above 39 weeks of gestation
4.Patients with Mallampati grade 1 and 2
5. Who are willing to participate for this study
Exclusion Criteria
1.Eclampsia
2.Antepartum Haemorrhage
3.Foetal distress absolute contraindication to spinal anaesthesia
4.Patient refusal
5.Patient receiving any nasal decongestant within 24hrs prior to surgery
6.Having nasal congestion
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effectiveness of Phenylephrine via different route in preventing spinal induced hypotension in emergency LUCSTimepoint: 6 month after approval of ethical committee
- Secondary Outcome Measures
Name Time Method To Observe any other side effect of the drug for example - nasal congestion, bradycardiaTimepoint: 6 month after approval of ethical committee