- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04650308
Sex Differences in Neuropeptide Y Serum, But Not in Fat Intake and Body Mass Index
November 30, 2020 updated by: DINA KEUMALA SARI, Universitas Sumatera Utara
One's appetite has a role in controlling food intake and maintaining energy balance, but its effect on body metabolism related to obesity is still questionable.
The purpose of this study was to determine the levels of neuropeptide Y in healthy people and to see differences in gender and anthropometric parameters.
The hypothesis of this study was that there would be differences in neuropeptide Y levels in groups with gender and anthropometric parameter differences.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
One's appetite has a role in controlling food intake and maintaining energy balance, but its effect on body metabolism related to obesity is still questionable.
The purpose of this study was to determine the levels of neuropeptide Y in healthy people and to see differences in gender and anthropometric parameters.
The hypothesis of this study was that there would be differences in neuropeptide Y levels in groups with gender and anthropometric parameter differences.
This study was a cross-sectional study involving 62 study subjects, male and female, who did not have chronic diseases or metabolic disorders.
This research was conducted from April to September 2020.
The parameters examined in this study were neuropeptide Y levels and anthropometric parameters.
The statistical analysis performed was the Mann-Whitney test to see the differences between groups.
The mean age of the research subjects was 40.48 ± 10.85 years, with the same ethnic distribution.
The distribution of men and women was more women than men.
Based on anthropometric examination, it was found that obesity nutritional status was more common in the female group than in the male group; however, serum neuropeptide Y levels were found to be significantly different between male and female groups (male group was higher).
Study Type
Interventional
Enrollment (Actual)
62
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North Sumatra
-
Medan, North Sumatra, Indonesia, 20155
- Faculty of Medicine Universitas Sumatera Utara
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- healthy groups for Neuropeptide Y Serum diagnosis
Exclusion Criteria:
- Non-healthy groups for Neuropeptide Y Serum diagnosis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Healthy group
healthy men and women aged 20-60 years old.
|
This examination was conducted by drawing blood serum from research subjects and performing centrifugation with 2000-3000 revolutions per minute (RPM) for 20 minutes.
Furthermore, we carried out blood serum tests to check neuropeptide Y levels using the Human Neuropeptide Y Enzyme-link Immunosorbent Assay (ELISA) kit
|
|
Active Comparator: Non-healthy group
pregnant women, nursing mothers, impaired kidney and liver function, chronic disease, or other metabolic disorders.
|
This examination was conducted by drawing blood serum from research subjects and performing centrifugation with 2000-3000 revolutions per minute (RPM) for 20 minutes.
Furthermore, we carried out blood serum tests to check neuropeptide Y levels using the Human Neuropeptide Y Enzyme-link Immunosorbent Assay (ELISA) kit
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
levels of neuropeptide Y
Time Frame: up to 2 weeks
|
up to 2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 2, 2020
Primary Completion (Actual)
June 17, 2020
Study Completion (Actual)
September 10, 2020
Study Registration Dates
First Submitted
November 23, 2020
First Submitted That Met QC Criteria
November 30, 2020
First Posted (Actual)
December 2, 2020
Study Record Updates
Last Update Posted (Actual)
December 2, 2020
Last Update Submitted That Met QC Criteria
November 30, 2020
Last Verified
November 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- USumateraUtara 2
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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