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Exploration of the "Blood and Water Coexisting Disease" Theory in Endometriosis: Scientific Insights and Intervention Research via Glucose-Lipid Metabolic Reprogramming

Exploration of the "Blood and Water Coexisting Disease" Theory in Endometriosis: Scientific Insights and Intervention Research via Glucose-Lipid Metabolic Reprogramming

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123043
Enrollment
Unknown
Registered
2026-04-21
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Endometriosis

Interventions

Healthy control group (non-endometriosis control group):None

Sponsors

Guangdong Second Provincial General Hospital (Guangdong Provincial Emergency Hospital)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Endometriosis Group 1. Meets Western and Traditional Chinese Medicine diagnostic criteria; dysmenorrhea score <=8 points 2. Aged 20-45 years, premenopausal women, with regular menstrual cycles (23-37 days) 3. Able to provide informed consent 4. Patients with pelvic endometriosis combined with adenomyosis may be included Healthy Control Group 1. Aged 20-45 years 2. Regular menstrual cycles: defined as a cycle length of 21-35 days, with cycle variation <7 days 3. No history of endometriosis 4. Signed informed consent: voluntarily participates in the study and is able to understand and sign the informed consent form

Exclusion criteria

Exclusion criteria: Endometriosis Group 1. Patients planning to undergo surgery in the near future 2. Patients with pelvic infection or other severe gynecological diseases (such as gynecological malignancies) 3. Patients with severe primary diseases involving the cerebrovascular, hepatic, renal, hematopoietic, thyroid systems, or malignancies; patients with psychiatric disorders; patients with epilepsy 4. Serum CA125 >200 U/ml 5. Ovarian endometrioma >5 cm, or accompanied by other types of ovarian cysts or solid masses; uterine fibroids >5 cm 6. Dysmenorrhea caused by other reasons; or any situation deemed by the researcher to affect participant safety Healthy Control Group 1. Current or history of any benign or malignant gynecological tumors: such as uterine fibroids (symptomatic or diameter >3 cm), ovarian cysts (excluding physiological cysts), adenomyosis, cervical lesions, ovarian cancer, etc. 2. Currently pregnant or breastfeeding; postmenopausal status; presence of unexplained pelvic masses or abnormal uterine bleeding 3. Use of hormonal medications within 3-6 months prior to enrollment 4. Severe systemic diseases: uncontrolled endocrine disorders (such as hyper/hypothyroidism, diabetes), autoimmune diseases (such as systemic lupus erythematosus, rheumatoid arthritis), cardiovascular diseases, hepatic or renal insufficiency, etc. 5. Long-term use of anti-inflammatory or analgesic drugs (such as non-steroidal anti-inflammatory drugs, opioids); history of psychiatric disorders or substance abuse 6. Any other situation deemed by the researcher that may affect study assessment or participant safety

Design outcomes

Primary

MeasureTime frame
Serum CA125;Tongue characteristics;Glycometabolism and Lipid Metabolism Related Indicators;Pain Visual Analogue Scale (VAS) Score;

Countries

China

Contacts

Public ContactZheng Weilin

Guangdong Second Provincial General Hospital (Guangdong Provincial Emergency Hospital)

1150654956@qq.com+86 20 39318681

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026