CTRI/2018/05/014242
Active, not recruiting
未知
Continuous invasive blood pressure monitoring following low dose spinal anaesthesia for caesarean delivery in women with valvular heart disease: An observational study.
Department of Anaesthesia and Intensive Care PGIMER0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Women undergoing caesarean delivery having mild to moderate valvular heart disease
- Sponsor
- Department of Anaesthesia and Intensive Care PGIMER
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\)Mild/moderate mitral stenosis: Mitral valve area \>\= 1cm2,mean pressure gradient across mitral valve\<\= 12mmHg, Pulmonary artery mean pressure \<\= 50mmHg, New York Heart Association (NYHA) functional classificationâ??Class I and Class II
- •2\)Mild/moderate aortic stenosis: Peak systolic pressure gradient across aortic valve \<65 mmHg and ejection fraction \>50%, New York Heart Association (NYHA)functional classificationâ?? Class I and
Exclusion Criteria
- •1\)Severe mitral stenosis with mitral valve area \<1 cm2,NYHA III/IV, hypotension, pulmonary edema
- •2\)Severe aortic stenosis with peak gradient of \>65mmHg, ejection fraction \<50%
- •3\)Any valvular lesion with NYHA functional class III/IV, pulmonary edema, atrial fibrillation with ventricular rate \>100/ min, ejection fraction \<50%.
- •4\)Anemia with Hb \<9gm % (according to institution standard)
Outcomes
Primary Outcomes
Not specified
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