Observational Study of the Association Between Food Intake and Endometrial Polyps

February 28, 2024 updated by: qinxiu zhang

A Cross-sectional Observational Study of the Association Between Food Intake and Endometrial Polyps

There are currently no studies evaluating the association between diet and the incidence of endometrial polyps. We aim to evaluate the association to provide more recommendations for the early prevention of endometrial polyps.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

The incidence of endometrial polyps is closely related to daily diet and living habits. Due to the excessive use of food additives, the content of some common dietary hormones exceeds the standard, causing irreversible effects on female growth and development.

The daily diet structure is closely related to women's health, and the enrichment of estrogen in common drinks may cause adverse effects such as premature puberty in women, abnormal thyroid function, and changes in uterine structure. Therefore, the researchers conducted a retrospective analysis of patients with endometrial polyps and normal women to compare the associations and differences between daily diet and disease.

Study Type

Observational

Enrollment (Estimated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study period will include all patients who attended gynecological outpatient clinics between March 1, 2024 and May 1, 2024

Description

Inclusion Criteria:

  • Consistent with the international clinical diagnosis of endometrial polyps.Can complete content recall alone.

Exclusion Criteria:

  • No other mental diseases. Not associated with other major diseases, including tumors, immune system diseases

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
healthy group (HG)

Participants were grouped according to their basic conditions without any intervention.

no intervention It's only observational study. No interventions.
Other: No interventions.
It's only observational study.
case group（PG）

Participants were grouped according to their basic conditions without any intervention.

no intervention It's only observational study. No interventions.
Other: No interventions.
It's only observational study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hormonal dietary intake
Time Frame: Within the past 1 year
Daily dietary intake questionnaire was used to evaluate.Weekly intake of milk tea, coffee, beverage, etc
Within the past 1 year
Comparison of daily living habits
Time Frame: Within the past 1 year
Sleep, exercise, and other basic information were assessed based on a daily habits questionnaire.
Within the past 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

qinxiu zhang

Investigators

  • Study Director: Qinxiu Zhang, Hospital of Chengdu University of Traditional Chinese Medicine

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 (Estimated)

March 1, 2024

Primary Completion (Estimated)

April 1, 2024

Study Completion (Estimated)

May 1, 2024

Study Registration Dates

First Submitted

February 22, 2024

First Submitted That Met QC Criteria

February 28, 2024

First Posted (Estimated)

March 6, 2024

Study Record Updates

Last Update Posted (Estimated)

March 6, 2024

Last Update Submitted That Met QC Criteria

February 28, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CDUTCM20240223

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Readers can access the survey data through a public data platform

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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