Skip to content

Investigating biochemical parameters and functional capacity in obese patients with coronary artery occlusive disease trained with a short-term diet

Investigating biochemical parameters and functional capacity in obese patients with coronary artery occlusive disease trained with a short-term diet

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230731058983N1
Enrollment
100
Registered
2023-11-14
Start date
2023-11-17
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Condition 1: coronary artery disease. Condition 2: obesity. Condition 3: blood pressure. Condition 4: diabet. Atherosclerotic heart disease of native coronary artery Obesity due to excess calories Examination of blood pressure Type 2 diabetes mellitus

Interventions

Intervention 1: Intervention group: All patients in the intervention group are provided with a three-month short-term balanced diet by a nutritionist. This visit will last for at least half an hour an

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: coronary artery disease with at least 50% stenosis BMI more than 30 patient satisfaction Age above 18 years

Exclusion criteria

Exclusion criteria: coronary artery disease with less than 50% stenosis BMI less than 30 patients with hyperthyroidism Any type of musculoskeletal and rheumatologic disease that prevents patients from walking Age under 18 years Any known cancers in patients Known chronic kidney disease in patients (such as types of glomerulonephritis or patients undergoing routine dialysis) Known liver disease in patients (such as types of viral hepatitis and autoimmune hepatitis) Immunocompromised patients People with disabilities Bedridden people

Design outcomes

Primary

MeasureTime frame
Distance covered in the 6 Minutes Walking test. Timepoint: at 0 and 3 months after the intervention in the two investigated groups. Method of measurement: Checking the distance traveled during 6 minutes.;Level of fasting blood sugar. Timepoint: Time zero and 3 months after the intervention in the two studied groups. Method of measurement: Hospital laboratory kit.;Serum level of lipid profile (LDL, Chol, TG, HDL). Timepoint: Time zero and 3 months after the intervention in the two studied groups. Method of measurement: Hospital laboratory kit.;Serum levels of SGOT and SGPT. Timepoint: Time zero and3 months after the intervention in the two studied groups. Method of measurement: Hospital laboratory kit.;BMI and waist circumference. Timepoint: Time zero and 3 months after the intervention in the two studied groups. Method of measurement: scale and meter.;HbA1C. Timepoint: Time zero and 3 months after the intervention in the two studied groups. Method of measurement: Hospital laboratory kit.;Average systolic and diastolic blood pressure. Timepoint: Time zero and 3 months after the intervention in the two studied groups. Method of measurement: blood pressure device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Akbari

Birjand University of Medical Sciences

Akbari.Azad@gmail.com+98 56 3162 6000

Outcome results

None listed

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