Factors Associated With Pre-hypertension Among Children With Type 1 Diabetes Mellitus
NCT ID: NCT07172399
Last Updated: 2025-09-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
60 participants
OBSERVATIONAL
2025-07-26
2026-08-05
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
A Clinical Study of the Performance of a Glucose Blinding Protein-Based Continuous Glucose Monitor (GBP CGM)
NCT01469715
Validation of a 13C Glucose Breath Test Compared With the Euglycaemic Clamp Test
NCT04623320
Feasibility and Effectiveness of Real-time, Remote Continuous Glucose Monitoring in Adolescents With Poorly Controlled Type 1 Diabetes
NCT04540536
Hormone Responses During Hypoglycemia and the Accuracy of Continuous Glucose Monitors
NCT00607139
Continuous Glucose Monitoring in Women With Type 1 Diabetes in Pregnancy Trial
NCT01788527
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* BP will be measured using a calibrated, automated oscillometric device suitable for pediatric use.
* Appropriate cuff size will be used based on mid-arm circumference.
* Blood pressure will be measured in the non-dominant arm.
* BP will be measured three times on at least two different occasions, after 5 minutes of rest, in a seated position.
* The average of the readings will be recorded.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
blood sampling
blood samples will be taken to discover if there is hyperlipedemia,hyperthrodism or acute kidney injury
• BP will be measured using a calibrated, automated oscillometric device suitable for pediatric use.
All the study participants will be examined for assessment of the height and weight using calibrated equipment, Body Mass Index ,blood pressure will be measured.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
\-
6 Years
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sohag University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Aya Mohamed Ibrahim
aya ibrahim
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sohag university hospital
Sohag, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Soh-Med--25-7-6MS
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.