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Clinical Study on the Performance of Hysterosalpingography Imaging

Clinical Study on the Performance of Hysterosalpingography Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108357
Enrollment
Unknown
Registered
2025-08-28
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Diagnosis of tubal patency

Interventions

Observation group:None

Sponsors

Shenzhen Maternity & Child Healthcare Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients who are clinically required to undergo ultrasound examination or diagnosis of the uterus and appendages; 2. Women of childbearing age aged 18~49 years; 3. 3~7 days after menstruation is clean, and 3 days before the examination; 4. Volunteer to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Acute inflammation of internal and external reproductive organs, severe trichomoniasis or candida vaginitis; 2. Severe cervical chronic inflammation or excessive discharge; 3. Active pelvic tuberculosis; 4. Suspected malignant lesions of the cervix or uterine cavity; 5. Those who are allergic to any component in the ultrasound contrast agent; 6. Pregnant and lactating women; 7. Patients with systemic or cardiopulmonary vascular diseases, hyperthyroidism and uncontrolled hypertension; 8. Those who have mental illness and cannot cooperate with the examination; 9. The investigator thinks that it is not suitable to participate in this research.

Design outcomes

Primary

MeasureTime frame
Excellent rate of real-time 3D contrast-enhanced images;

Secondary

MeasureTime frame
Excellent rate of two-dimensional and static three-dimensional contrast images;

Countries

China

Contacts

Public ContactShengli Li

Shenzhen Maternity & Child Healthcare Hospital

lishengli@126.com+86 13500052555

Outcome results

None listed

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