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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05521932
Other study ID # Ruijin Wu
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 20, 2022
Est. completion date December 31, 2024

Study information

Verified date May 2024
Source Women's Hospital School Of Medicine Zhejiang University
Contact Ruijin Wu, M.D.
Phone 0086-0571-87061501
Email wurj@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Normal endometrial repair occurs without scar formation; however, in some women, these normal repair mechanisms are aberrant, resulting in intrauterine adhesion (IUA) formation. Intrauterine adhesion (IUA) is one of the common causes of secondary infertility, accounting for approximately 8% of disease etiologies while the pathogenesis of IUA remains unclear. Organoids derived from IUA endometrium can be used as excellent models to study IUA due to genetically stable passage and the characteristics of simulating the microenvironment of the uterine cavity.


Description:

Intrauterine adhesion (IUA), also known as Asherman syndrome, is a common gynecological disease, the main clinical manifestations are oligomenorrhea, amenorrhea, recurrent miscarriage and infertility, which seriously endanger the reproductive function of women of childbearing age . Trauma and infection are the most common and important causes of IUA. At present, the incidence of infertility in the population is about 9%-18%. According to the prediction of World Health Organization (WHO), IUA will become the third largest disease after tumor and cardiovascular disease in the future. Organoids are 3D self-organized structures that could derived from tissue and have a variety types of cell, and mimic the target organ in structure and function. They have the ability to proliferate, differentiate and self-renew. Maintain genetic stability and reproduce some physiological functions. Organoids forms closer intercellular connections and biological communication than 2D cultured cells, and is better used to simulate the occurrence process and physiological and pathological states of organs and tissues. Therefore, investigator proposed to establish a IUA organoids bio-bank for further investigation of pathogenesis of IUA and seek for personalized therapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - clinical diagnosis of IUA - undergoing hysteroscopic surgery for treatment Exclusion Criteria: ·receiving sex hormone therapy in the three months before surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
endometrium collected
endometrium tissue collected following adhesiolysis surgery

Locations

Country Name City State
China Women's Hospital Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Women's Hospital School Of Medicine Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary IUA organoid formation efficiency Establishment IUA organoid from patient-derived endometrium tissue. The following outcome measure would be calculated:
the formation efficiency of organoid
2 years
Primary IUA organoid proliferative rate Establishment IUA organoid from patient-derived endometrium tissue. The following outcome measure would be calculated:
the proliferative rate of organoid
2 years
Secondary IUA organoid identification the IUA organoid identification will assessed by the following method: Identification of cell type and ultrastructure of IUA organoid by pathological staining and electron microscope. 2 years
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