Skip to content

Peripheral combined central dual-target magnetic stimulation for rehabilitation of chronic pelvic pain syndrome with psychosomatic disorders: Randomized Controlled Trial

Peripheral combined central dual-target magnetic stimulation for rehabilitation of chronic pelvic pain syndrome with psychosomatic disorders: Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078761
Enrollment
Unknown
Registered
2023-12-18
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

chronic pelvic pain syndrome

Interventions

dual-targeted magnetic stimulation group:Repetitive transcranial magnetic stimulation combined with repetitive trans sacral 3 nerve magnetic stimulation
peripheral magnetic stimulation group:Sham transcranial magnetic stimulation combined with repetitive trans sacral 3 nerve magnetic stimulation
sham stimulation group:Use a coil that does not produce a magnetic field, only emits sound, and perform sham stimulation first through the scalp and then through the sacral 3 area.

Sponsors

Chengdu Anorectal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Compliance with the European Association of Urology (EAU) guidelines for chronic pelvic pain (2022 edition) CPPS diagnostic criteria. (2) Age: 18-60 years old. (3) Definite diagnosis of anxiety or depression. (4) Gynaecological examination and auxiliary examination did not reveal clear pathological changes. (5) Obtained informed consent and entered the study voluntarily. (6) Not receiving any treatment modality within 3 months prior to the visit. (7) Patients gave informed consent and voluntarily participated in this study.

Exclusion criteria

Exclusion criteria: (1) Patients in the acute phase of systemic and intracranial haemorrhagic diseases. (2) Those with combined cardiovascular, cerebrovascular, hepatic, renal, respiratory and haematopoietic systems and other serious primary diseases, malignant tumours and/or other progressive underlying diseases. (3) Patients with metal heart membranes, pacemakers, intracranial metal implants, lumbosacral metal implants and implantable electronic devices. (4) Those with intracranial or lumbosacral infections. (5) Patients with unstable vital characteristics. (6) Patients with adverse reactions to magnetic therapy. (7) Patients with abnormal autonomic reflexes. (8) Combined cognitive dysfunction can not cooperate. (9) Pregnant and lactating women. (10) Patients with previous history of diabetes mellitus, alcoholism and toxicity and any other diseases that cause peripheral nerve damage.

Design outcomes

Primary

MeasureTime frame
Pelvic Pain Assessment Scale;Phenotype classification system (UPOINTS);

Secondary

MeasureTime frame
Depression Anxiety and Stress Scale;SF-36 Quality of Life Scale;

Countries

China

Contacts

Public ContactXiangdong Yang

Chengdu Anorectal Hospital

xiangdongyang2011@163.com+86 158 2825 0622

Outcome results

None listed

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