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Comparison and causation of anxiety in patients with endometriosis cysts and benign ovarian cysts: a cross-sectional case-control study

Comparison and causation of anxiety in patients with endometriosis cysts and benign ovarian cysts: a cross-sectional case-control study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078143
Enrollment
Unknown
Registered
2023-11-29
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

Endometriosis

Interventions

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: I. Study Group 1 In line with the clinical diagnosis of EMS cysts; 2 did not give birth, have a desire to give birth; 3 Patients of the gynecological outpatient department of the Third Affiliated Hospital of Sun Yat-sen University; 4 Willing to cooperate with the doctor to complete the questionnaire survey; 5 Sign informed consent; Age 6:20-35 years old. II. Control group A 1 Non-EMS patients who met the diagnosis of benign ovarian cyst; 2 did not give birth, have a desire to give birth; 3 Patients of the gynecological outpatient department of the Third Affiliated Hospital of Sun Yat-sen University; 4 Willing to cooperate with the doctor to complete the questionnaire survey; 5 Sign informed consent; Age 6:20-35 years old. III. Control group B 1. Women with normal physical examination results at the physical examination center; 2 did not give birth, have a desire to give birth; 3 Willing to cooperate with the doctor to complete the questionnaire survey; 4 Sign informed consent; 5 years old: 20-35 years old

Exclusion criteria

Exclusion criteria: 1 Patients with a history of anxiety; Persons with neurological and/or cognitive problems, inability to understand the nature or scope of the study, or inability to comply with medical orders; 3 Patients with other chronic pain other than the reproductive system; 4. History of organic disease; 5 Unwilling to sign informed consent.

Design outcomes

Primary

MeasureTime frame
self-rating anxiety scale;

Secondary

MeasureTime frame
Self-rating depression Scale;

Countries

China

Contacts

Public ContactYu Zhang

The Third Affiliated Hospital of Sun Yat-sen University

zhangyu6@mail.sysu.cn.com+86 13 688 870 2226

Outcome results

None listed

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