Skip to content

A clinical comparative study of two different endometrial cell samplings for the diagnosis of endometrial lesions

A clinical comparative study of two different endometrial cell samplings for the diagnosis of endometrial lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800020281
Enrollment
Unknown
Registered
2018-12-22
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

endometrial diseases

Interventions

Gold Standard:diagnosis of endometrial histo-pathology
Index test:the&#32
cyto-pathological&#32
siagnosis&#32
of&#32
two&#32
sampler:&#32
Li&#32
and&#32
Tao&#32

Sponsors

First Affiliated Hospital, Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. postmenopausal uterine bleeding; 2. endometrial thickness>5mm,with or withnot heterogeneous and hypoechoic internal echoes; 3. abnormal uterine bleeding during peri-menopause; 4. efficacy evaluation of endometrial hyperplasia; 5. abnormal uterine bleeding during HRT; 6. estrogen alone during HRT; 7. abnormal uterine bleeding with risk of endometrialcancer(obesity/hypertension/diabetes/tamoxifen use/family history of endometrial cancer/Lynch syndrome).

Exclusion criteria

Exclusion criteria: 1. Acute inflammation of the reproductive system (except atrophic vaginitis); 2. Endogenous cervical cancer; 3. coagulation abnormalities and others system hematological system disorders effect on blood coagulative; 4. Pregnancy or suspicious pregnancy; 5. body temperature > 37.5 degree C.

Design outcomes

Primary

MeasureTime frame
the accuracy of cyto-pathology;

Countries

China

Contacts

Public ContactQiling Li

First Affiliated Hospital, Xi'an Jiaotong University

liqiling@mail.xjtu.edu.cn+86 18991232838

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026