RecruitingPhase 3ACTRN12613000495729

Dexmeditomedine for mitral valve replacement

dexmeditomedine for heart rate control during mitral valve replacement for mitral stenosis a randomised controlled double blind study


Sponsor

south valley university -Qena university hospital

Enrollment

70 participants

Start Date

Nov 5, 2011

Study Type

Interventional

Conditions

Summary

testing the efficacy and safety of dexmeditomedine in controlling heart rate in patients with tight mitral stenosis subjected to mitral valve replacement during the prebypass period


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 60 Yearss

Inclusion Criteria1

  • patients ASAI&II with tight ( less than one centimeter ) mitral stenosis aged 18-60 years of age scheduled for mitral valve replacement

Exclusion Criteria1

  • age above or below 18-60 years , mitral valve area more than one centimeter, renal or hepatic dysfunction , cardiac medications that affect heart rate

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Interventions

70 patients scheduled for mitral valve replacement divided equally into two groups were studied in this randomized controlled double blind study ; Group D : received (after induction of anesthesia) de

70 patients scheduled for mitral valve replacement divided equally into two groups were studied in this randomized controlled double blind study ; Group D : received (after induction of anesthesia) dexmeditomedine 1ug/kg bolus dose over 10 minutes followed by an infusion of 0.5 ug/kg/h till the start of cardiopulmonary bypass. Group F: received saline bolus ( after induction of anesthesia ) and infusion of saline till the start of cardiopulmonary bypass instead of dexmeditomedine .Anesthetic management for both groups was the same.


Locations(1)

Qena - upper Egypt, Egypt

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ACTRN12613000495729