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Therapeutic effect of glargine combind aspart comparing regiment NPH combind regular for treatment patients with type 1 diabetes

Regiment glargine combind aspart comparing regiment NPH combind regular for treatment patients with type 1 diabetes that reffered to pediatric medical center 1390;clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203079224N1
Enrollment
40
Registered
2012-05-28
Start date
2012-05-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Diabetes Mellitus. Insulin-dependent diabetes mellitus

Interventions

Intervention 1: Patients who are treated with new drugs, will received glargine insulin as basal insulin once day( before bedtime)and Sparta insulin as rapid effect of insulin with meals 3 times a day
Treatment - Drugs
Patients who are treated with new drugs, will received glargine insulin as basal insulin once day( before bedtime)and Sparta insulin as rapid effect of insulin with meals 3 times a day (breakfast, lun
NPH insulin-treated patients in the control group received twice a day ( before breakfast and dinner) with short-acting insulin regular three times daily( 30 minute before breakfast, lunch, dinner).

Sponsors

Tehran University of Medical Sciences Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 11 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 6 to 11 years old; patient with diagnosis of type 1diabetes mellitus that under treatment of insulin at least 6 month; Body Mass Index below the 90th percentile at baseline and having the desire and ability to measure blood glucose self monitoring (SMBG) using glucometer devices. Exclusion criteria: diabetic patients with diabetes who have other mental and physical disorders; patients who did not complete the study period and patients with diabetes are not suitable for regular tracking and check.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
HbA1c. Timepoint: Every 3 month. Method of measurement: Labratory test.;Lipid profile. Timepoint: Every 6 month. Method of measurement: Laberatory test; mg/dl.;Fasting blood glucose. Timepoint: Everyday. Method of measurement: Laberatory test; mg/dl.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Aria Setoodeh

Tehran University of Medical Sciences

setoodeh@tums.ac.ir ;arset59@gmail.com+98 21 6694 8443

Outcome results

None listed

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