Determination of Risk Factors for the Development of Obesity and Hypertension in Children According to Perinatal Programming of Metabolism
|
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: NCT04611412 |
|
Recruitment Status :
Recruiting
First Posted : November 2, 2020
Last Update Posted : November 2, 2020
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment |
|---|---|
| Metabolic Syndrome | Other: Risk Factors |
| Study Type : | Observational |
| Estimated Enrollment : | 55 participants |
| Observational Model: | Cohort |
| Time Perspective: | Retrospective |
| Official Title: | Determination of Risk Factors for the Development of Obesity and Hypertension in Children According to Perinatal Programming of Metabolism |
| Estimated Study Start Date : | December 15, 2020 |
| Estimated Primary Completion Date : | December 30, 2023 |
| Estimated Study Completion Date : | January 2, 2024 |
| Group/Cohort | Intervention/treatment |
|---|---|
|
1 group
Group I consisted of 17 people (16.83%) with a uniform type of obesity
|
Other: Risk Factors
BMI in children and adolescents was compared with percentile charts developed by who for children from 5 to 19 years of age (WHO Growth Reference, 2007). Body mass index was defined as the ratio of body weight (in kg) to body length in the supine position or height in the standing position (m2). |
|
2 group
Group II included 38 children with AO, and 20 of them had normal BLOOD pressure
|
Other: Risk Factors
BMI in children and adolescents was compared with percentile charts developed by who for children from 5 to 19 years of age (WHO Growth Reference, 2007). Body mass index was defined as the ratio of body weight (in kg) to body length in the supine position or height in the standing position (m2). |
- Risk factors of metabolic syndrome [ Time Frame: up to 36 months ]
A retrospective, cohort study of 55 children aged 12 to 18 years with exogenous constitutional obesity will be conducted Children with exogenous-constitutional obesity were divided by the presence of abdominal (visceral) obesity and the presence of hypertension.
Parents will be interviewed and medical records (forms 003/y and 112) of children with exogenous constitutional obesity will be analyzed. Also, on the basis of a specially developed questionnaire, children with exogenous constitutional obesity were surveyed. When conducting a survey of children and their parents, the following factors will be of particular importance: heredity, pregnancy, weight and body length at birth, the nature of nutrition in the first two years of life, eating habits, and physical activity.
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: | 12 Years to 18 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- SDS (standart deviation score) of body mass index (BMI) ranging from +2.0 to +3.0
Exclusion Criteria:
- secondary obesity and overweight genetic syndromes,
- refusal of the child and/or parents to be examined
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): NCT04611412
| Uzbekistan | |
| Samarkand State Medical Institute | Recruiting |
| Samarkand, Uzbekistan, 140100 | |
| Contact: Lilya M Garifulina, PhD +998915497971 ms.garifulina77@mail.ru | |
| Responsible Party: | Samarkand State Medical Institute |
| ClinicalTrials.gov Identifier: | NCT04611412 |
| Other Study ID Numbers: |
Project #4 |
| First Posted: | November 2, 2020 Key Record Dates |
| Last Update Posted: | November 2, 2020 |
| Last Verified: | October 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Plan Description: | Study participants will perform all types of medical and diagnostic activities |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
Metabolic Syndrome children obesity |
|
Hypertension Obesity Metabolic Syndrome Vascular Diseases Cardiovascular Diseases Overnutrition Nutrition Disorders |
Overweight Body Weight Insulin Resistance Hyperinsulinism Glucose Metabolism Disorders Metabolic Diseases |

