Skip to content

Use of Dexmedetomedine to complement the benefit of total anesthetic stability in patients who are undergoing heart surgeries.

Dexmedetomedine as a perioperative adjunct in patients undergoing cardiac surgery - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075359
Enrollment
153
Registered
2024-10-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: I01- Rheumatic fever with heart involvement

Interventions

Intervention1: Dexmedetomidne at 05 ug/kg/hr: This was the adjuvant sedative given in these patients. This will be given INTRAVENOUSLY, at 5ug/kg/hr. This will be given from the onset of induction of

Sponsors

Dr Sanjeeta Umbarkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing valvular cardiac surgery

Exclusion criteria

Exclusion criteria: Preoperative treatment with morphine or its derivatives including tramadol in the 15 days preceding the inclusion visit Pre-existing high-degree conduction disorder Oxygen therapy prior to inclusion Heart failure with LVEF less than 40 percent BMI more than 35 Myocardial suffering in the 5 days preceding surgery Patient in shock Known adrenal insufficiency and or long-term systemic corticosteroid treatment equivalent to hydrocortisone hemisuccinate more than 20 mg per day Long-term non-invasive ventilation including for obstructive sleep apnea syndrome Any antecedent or active practices of drug addiction Contraindication to one of the experimental and or nonexperimental treatment like dexmedetomidine lidocaine dexamethasone ketamine remifentanil or morphine Acute cerebrovascular pathology Severe hepatic insufficiency with factor V level less than 50 percent Pre-existing cognitive disorders Pregnant or parturient or breastfeeding woman Person deprived of liberty by an administrative or judicial decision or person placed under judicial protection under guardianship or guardianship Patient participating in another drug trial or having participated in another drug trial within 1 month before randomization

Design outcomes

Primary

MeasureTime frame
To assess the effects of Dexmedetomidine on hemodynamics and depth of anesthesia in patients undergoing valvular heart replacement surgeriesTimepoint: Baseline post induction after Sternotomy after pericardiotomy 5 minutes after protamine administration end of surgery

Secondary

MeasureTime frame
To assess duration of ICU stay & incidences of postoperative complications which received Dexmedetomidine perioperativelyTimepoint: Admission to ICU after surgery upto 30 days status of patient

Countries

India

Contacts

Public ContactDr Sanjeeta Umbarkar

Seth GS Medical college and KEM Hospital

sanjeeta69@yahoo.com9323273435

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026