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A study to assess the effect of supplemenatation of beta-hydroxy-beta-methyl butyrate (HMB) in patients undergoing heart surgery with cardiopulmonary bypass (CPB)

A study to assess the outcome of preoperaive supplemenatation of beta-hydroxy-beta-methyl butyrate (HMB) in cardiac surgery using cardiopulmonary bypass (CPB)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/051341
Enrollment
40
Registered
2023-04-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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

Interventions

Intervention1: Hydroxy Methyl Butyrate (HMB) Group: Hydroxy Methyl Butyrate (HMB) 1.5g oral will be supplementated everyday for two weeks before the cardiac surgery. Control Intervention1: Control gro

Sponsors

The Madras Medical Mission, Chennai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective Cardiac surgery using cardiopulmonary bypass Patients with adequate LV function Patients with mild to moderate LV dysfunction

Exclusion criteria

Exclusion criteria: Patients with Severe LV dysfunction Preexisting kidney disease Preexisting liver disease Smoking, drug/alcohol abuse Hepatitis B & C infection Endocrine disorders Autoimmune disorders Patients already on protein supplementation Offpump cardiac surgeries Patient refusal

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is to determine whether preoperative supplementation of Beta-Hydroxy-Beta-Methyl butyrate (HMB) improves the outcome in the elective cardiac surgery on cardiopulmonary bypass (CPB).Timepoint: The patient is assessed one day before supplemenation and 2 weeks after supplementation, and again on the first post operative day

Secondary

MeasureTime frame
The secondary outcome of the study is to determine the duration of ICU stay, mechanical ventilation, wound infections and post op complications. Timepoint: The patient is assessed one day before supplementation and 2 weeks after supplementation and again on the first post operative day.

Countries

India

Contacts

Public ContactDr Rameez Raja

The Madras Medical Mission, Chennai

rameezonline@live.com9597173094

Outcome results

None listed

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