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Clinical Trials/CTRI/2018/05/014242
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
Department of Anaesthesia and Intensive Care PGIMER

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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