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Effect of oral aloe vera powder on type 2 diabetes

Evaluation the Effect of Oral Aloe Vera Administration on Fasting Plasma Glucose, Lipid Profile, Body Composition Components, Anthropometric Indices, and Blood Pressure Values in Patients with Diabetes Type 2

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200331046900N1
Enrollment
60
Registered
2020-06-24
Start date
2019-01-21
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

Type 2 diabetes. Type 2 diabetes mellitus without complications

Interventions

Intervention 1: Intervention group: The raw materials and raw materials required were purchased from Shiraz University of Medical Sciences School of Pharmacy with the advice and approval of a consulta

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: The desire to participate in the study Age range 18 to 69 years Diagnosis of type 2 diabetes by a specialist The minimum duration of type 2 diabetes is 6 months Weight constant over the past 6 months ( Self-report ) The type and dose of medications taken have been stable over the past 6 months

Exclusion criteria

Exclusion criteria: Allergy to aloe vera or products containing it Pregnancy and lactation Use of any dietary supplement in the last 6 months Smoking and addiction Acute heart disease, stroke, liver, kidney, gastrointestinal, thyroid and parathyroid disease, rheumatoid and infectious arthritis

Design outcomes

Primary

MeasureTime frame
Total cholesterol. Timepoint: Before the intervention and after the intervention. Method of measurement: Blood test.

Secondary

MeasureTime frame
Fasting blood sugar. Timepoint: Before and after the intervention. Method of measurement: Blood test.;Triglyceride. Timepoint: Before and after the intervention. Method of measurement: Blood test.;High-density lipoprotein. Timepoint: Before and after the intervention. Method of measurement: Blood test.;Low-density lipoprotein. Timepoint: Before and after the intervention. Method of measurement: Blood test.;Anthropometry. Timepoint: Before and after the intervention. Method of measurement: Scales, meters, calipers and .;Blood pressure. Timepoint: Before and after the intervention. Method of measurement: Blood pressure monitor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNajmeh Sadat Zareian Jahromi

Shiraz University of Medical Sciences

najmeh.zareayan@gmail.com+98 71 9101 1710

Outcome results

None listed

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