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A multicenter study for the evaluation of reproductive function in women using intelligent system

A multicenter study for the evaluation of reproductive function in women using intelligent system

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022222
Enrollment
Unknown
Registered
2019-03-30
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-04-01

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

Conditions

Reproductive dysfunction

Interventions

Intelligent evaluation system Group:Evaluated OR and ER using the intelligent system
Non-Intelligent evaluation system Group:Evaluated OR and ER using the normal method

Sponsors

the Third Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.The first IVF-ET cycle of COH (long-acting form of gonadotrophin releasing, GnRH-antagonist protocol or mild ovarian stimulation protocol); 2. Aged above 21 years.

Exclusion criteria

Exclusion criteria: 1. The patients of ovariectomy; 2. Ovarian cyst (no less than 3cm); 3. Serious diseases (organic heart disease with cardiac function of level III-IV, renal or liver disfunction, malignant tumor needs radiotherapy); 4. With other endocrine disease; 5. Suckling period; 6. Vaginal bleeding; 7. Acute sexually transmitted diseases; 8. Acute inflammation of the reproductive system.

Design outcomes

Primary

MeasureTime frame
the number of retrieved oocytes;implantation rate;

Countries

China

Contacts

Public ContactZhiyi Chen

Department of Ultrasound Medicine, the Third Affiliated Hospital of Guangzhou Medical University

winchen@vip.126.com+86 18928916615

Outcome results

None listed

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