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The Research of the Effect for Fu's Subcutaneous Needling in curing the Chronic Pelvic Pain :a randomized controlled study

The Research of the Effect for Fu's Subcutaneous Needling (FSN) in curing the Chronic Pelvic Pain(CPP)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006143
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-15
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Chronic Pelvic Pain

Interventions

Swaying movement Group:Only swaying movement
Reperfusion Approach:Only Reperfusion Approach
Conventional medical therapy:Ibuprofen tablets and Levofloxacin capsules
Swaying movement and Reperfusion Approach Group:Both Swaying movement and reperfusion approach

Sponsors

Foshan hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Patients who met the diagnostic criteria of chronic pelvic pain (CPP); 2. Patients Aged between 18 and 50; 3. The score of Visual analogue Scale (VAS) of lower abdomen pain =3 4. Participated in the project voluntarily and had signed the Informed Consent form. 5. Those who met the above criteria should pay attention to contraception during treatment

Exclusion criteria

Exclusion criteria: 1. Patients had Pelvic organ tumors or other organic disease history. 2. Patients with serious diseases such as cardiovascular, cerebrovascular, liver, kidney and hematopoietic system, acute trauma; 3. Persons suffering from acute infectious diseases or serious skin diseases that are not suitable for treatment; 4. Patients with malignant tumors and mental disorders; Difficult to follow up; 5. People with spontaneous bleeding tendency such as taking anticoagulants; 6. Pregnant and lactating women; 7. Refusal to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Abdominal superfical blood perfusion;Visual Analogue Scale;

Secondary

MeasureTime frame
Hospital Anxiety and Depression Scale,HADS;

Countries

China

Contacts

Public ContactFei Qi

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1393465907@qq.com18086487010

Outcome results

None listed

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