Probiotics Supplementation Effect on Glucose Homeostasis in Children With Type 1 Diabetes
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04579341 |
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Recruitment Status :
Recruiting
First Posted : October 8, 2020
Last Update Posted : October 8, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Diabetes Mellitus, Type 1 | Dietary Supplement: probiotics | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 70 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | The Effect of Probiotics Supplementation on Glucose Homeostasis, Lipid Profile and Interleukin (IL)-21 and IL-22 Levels in Children With Type 1 Diabetes: A Randomized Placebo-controlled Trial |
| Actual Study Start Date : | January 21, 2018 |
| Estimated Primary Completion Date : | October 28, 2020 |
| Estimated Study Completion Date : | November 10, 2020 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: probiotics arm
probiotics administered in addition to insulin regimen
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Dietary Supplement: probiotics
probiotics administration |
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No Intervention: control
regular insulin regimen
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- glycemic control [ Time Frame: 6 months ]HbA1C
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 5 Years to 18 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- T1D
Exclusion Criteria:
- other types of DM
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04579341
| Contact: Nouran Salah, MD | 01116603336 | niron85@hotmail.com |
| Egypt | |
| Ain Shams University | Recruiting |
| Cairo, Ramses, Egypt, 11375 | |
| Contact: amira adly, MD | |
| Ain Shams University | Recruiting |
| Cairo, Egypt, 11375 | |
| Contact: Amira Adly, MD | |
| Principal Investigator: | Amira Adly, MD | Ain Shams University |
| Responsible Party: | Nouran yousef, Dr, Ain Shams University |
| ClinicalTrials.gov Identifier: | NCT04579341 |
| Other Study ID Numbers: |
Probiotics |
| First Posted: | October 8, 2020 Key Record Dates |
| Last Update Posted: | October 8, 2020 |
| Last Verified: | October 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
| Product Manufactured in and Exported from the U.S.: | No |
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Diabetes Mellitus Diabetes Mellitus, Type 1 Glucose Metabolism Disorders Metabolic Diseases |
Endocrine System Diseases Autoimmune Diseases Immune System Diseases |

