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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04323683
Other study ID # 13/EM/0277
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2019
Est. completion date July 31, 2019

Study information

Verified date March 2020
Source University of Nottingham
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates the relationship between progesterone levels and endometrial gene expression


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date July 31, 2019
Est. primary completion date July 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Ages 18-35, regular menstrual cycles, the cycle length between 25 and 35 days, body mass index (BMI) between 18 - 25

Exclusion Criteria:

- History of infertility, history of pelvic pain or/and endometriosis, history of pelvic mass, history of hormonal therapy in the last 3 months

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
Microarray
High throughput technique for determining global gene expression of the condition of interest

Locations

Country Name City State
United Kingdom Queen's medical center Nottingham

Sponsors (1)

Lead Sponsor Collaborator
University of Nottingham

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Differentially expressed genes between women with low and normal progesterone Fold-change and p-value were used to determine differentially expressed genes using Partek software 2 months
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