Semi-quantitative assessment of pain in patients with adenomyosis by functional magnetic resonance

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100045373

Enrollment

Unknown

Registered

2021-04-13

Start date

2021-05-01

Completion date

Unknown

Last updated

2021-11-22

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

Conditions

Adenomyosis

Interventions

Gold Standard:Gynecological ultrasound.

Index test:Functional&#32

magnetic&#32

resonance&#32

imaging.

Eligibility

Sex/Gender

Female

Age

18 Years to 52 Years

Inclusion criteria

Inclusion criteria: 1.Reproductive age women,right handedness; 2.Women with ultrasonographic evidence of adenomyosis; 3.Dysmenorrhea >= 6 months.

Exclusion criteria

Exclusion criteria: 1.Woman who is pregnant or nursing; 2.Patients with other chronic pain; 3.Patients with severe cardiovascular and cerebrovascular diseases, liver and kidney diseases, hematological diseases and malignant tumors; 4.Contraindications of MRI; 5.Patients with mental and neurological diseases.

Design outcomes

Primary

Measure	Time frame
Functional connectivity;Numerical Pain Score;Anxiety Self-Rating Scale;Depression Self-Rating Scale;Pain related factors;	—

Countries

China

Contacts

Public ContactWang Guoyun

Qilu Hospital of Shandong University

wangguoy@sdu.edu.cn+86 18560081937

Outcome results

None listed

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