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Endometriosis specific cohort study

Endometriosis specific cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-17013289
Enrollment
Unknown
Registered
2017-11-08
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-11-13

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

Conditions

Endometriosis

Interventions

Case series:Nil

Sponsors

Guangzhou Women and Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Women diagnosed consistent with the criteria of endometriosis confirmed by surgery and pathology; 2. Reproductive women aged 18 to premenopausal years; 3. Women who accept follow-up visits, volunteer for this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with other serious diseases or severe liver and kidney dysfuntion; 2. Patients without informed consents; 3. Conditions such as mental diseases or other reasons.

Design outcomes

Primary

MeasureTime frame
completion rate of cohort establishment;completion rate of blood sample collection;completion rate of tissue sample collection;data integrity rate;loss to follow up rate;completion rate of image information collection;

Countries

China

Contacts

Public ContactHuang Yanqing

Guangzhou Women and Children's Medical Center

huangyanqing@gwcmc.org+86 13798109888

Outcome results

None listed

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