Clinical application of CD138 immunohistochemistry and ultrasound detection of subendometrial blood flow in chronic endometritis

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100047482

Enrollment

Unknown

Registered

2021-06-20

Start date

2021-07-01

Completion date

Unknown

Last updated

2022-02-21

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

Conditions

Repeated embryo implantation failure

Interventions

spontaneous abortion group:No

Infertility group:No

RIF group:No

RSA group:No

AUB group:No

Control Group:No

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Study group: 1. Patients undergoing IVF / ICSI / PGT in our center; 2. Patients with spontaneous abortion, repeated implantation failure or normal pregnancy. Control group: Patients with normal pregnancy requiring artificial abortion.

Exclusion criteria

Exclusion criteria: 1. Intrauterine effusion or intrauterine adhesions; 2. Uterine malformation.

Design outcomes

Primary

Measure	Time frame
routine pathology;hysteroscopy;Immunohistochemical examination;	—

Countries

China

Contacts

Public ContactLi Yubin

Reproductive Center of the First Affiliated Hospital of Sun Yat-Sen University

liyubin97200@163.com+86 13556067519

Outcome results

None listed

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