Skip to content

Clinical study of Xiao-liu formula on pelvic pain management in patients with endometriosis

linical study of Xiao-liu formula on pelvic pain management in patients with endometriosis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045119
Enrollment
Unknown
Registered
2021-04-07
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-11-08

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

Conditions

endometriosis

Interventions

experimental group:Xiaoliu formula

Sponsors

Shenzhen Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Patients who complaint with pelvic pain and meet the diagnostic criteria for endometriosis and with pelvic pain. 2. Women aged between 20 and 45 years with regular period. 3. Diameter of pelvic cyst should be under 5 cm in ultrasound scan if any. 4. Patients with normal results of complete blood count, urine and stool tests, liver function, kidney function and electrocardiogram. 5. No steroids treatment at least 3 months, no painkiller intake at least 2 weeks.

Exclusion criteria

Exclusion criteria: 1. Women who prepare to get pregnant within 6 months and who are in gestational or lactation period now. 2. Patients who are diagnosed as reproductive malignant tumor, acute cervicitis, acute and pelvic inflammation, urinary infection, lower digestive inflammation. 3. Possible malignancy indications of endometriosis: (1) Endometriosis in postmenopausal women with irregular pain pattern; (2) Diameter of ovary cyst over 10 cm; (3) Malignant sign under ultrasound scan; (4) Serum CA125 > 200U/ml.

Design outcomes

Primary

MeasureTime frame
Questionnaire;

Secondary

MeasureTime frame
serum CA-125;

Countries

China

Contacts

Public ContactCao Da'nong

Shenzhen Traditional Chinese Medicine Hospital

382587051@qq.com+86 13688806559

Outcome results

None listed

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