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Accurate evaluation and individualized treatment strategy of myofascial pelvic pain syndrome

Accurate evaluation and individualized treatment strategy of myofascial pelvic pain syndrome

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070036
Enrollment
Unknown
Registered
2023-03-31
Start date
2023-03-31
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Myofascial pelvic pain syndrome

Interventions

Case series:N/A

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients will be admitted to the study when they meet all of the following criteria: (1)Clinically confirmed myofascial pelvic pain: patients reported pelvic pain with a pain intensity rating of at least 4 of 10 on an 11-point numerical rating scale that persisted for at least 6 months; During physical examination, there were pain trigger points when pressing pelvic floor muscles (levator ani and obturator); (2)Women over 18 years old; (3)Ever had sex; (4)Did not receive any related treatment within one month prior to enrollment in the study; (5)informed consent.

Exclusion criteria

Exclusion criteria: Patients will be excluded from the study if they have any of the following conditions: (1) Patients with pain causing diseases (such as endometriosis, interstitial cystitis, etc.) diagnosed by physical examination and auxiliary examination; (2) Pregnant woman; (3) Patients with vaginal bleeding, vaginitis, acute pelvic inflammatory disease; (4) Patients with malignant tumors; (5) Patients with previous neurological, mental and pelvic floor related surgery history; (6) Patients with cardiac pacemaker, electric shock defibrillator, electrical stimulation intolerance; (7) Participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
NRS score;

Secondary

MeasureTime frame
Pain evaluation;Mental health;Quality of life;Patient satisfaction;Temperature of pelvic floor;Safety evaluation;

Countries

China

Contacts

Public ContactChen Juan

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

pumchcj@sina.com13521354364

Outcome results

None listed

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