chronic pelvic pain
Conditions
Interventions
UGPRF group :UGPRF
Sham group:Sham UGPRF
Sponsors
The First Affiliated Hospital of Jiamusi University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Female patients aged between 18 and 60 years with a history of CPP, but without obvious pelvic pathology checked by the laparoscopy. In addition, patients experienced CPP (NRS >= 4, at the range of 0-10) for more than 6 months prior to the recruitment. Pain location should be at pelvis or between and below anterior iliac crests; agree to use effective contraception if necessary to avoid pregnancy during the study period; All enrolled patients should be able to provide informed consent.
Exclusion criteria
Exclusion criteria: Patients have the conditions of only dysmenorrhoea, any pelvic pathology disorders, receiving pain medications or other therapies and unwilling to stop, breast feeding, pregnant, pain caused by the other conditions, such as gastrointestinal disorders, participating other clinical trials, or receiving the UGPRF 3 months prior to the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric Rating Scale (NRS); | — |
Secondary
| Measure | Time frame |
|---|---|
| 36-Item Short Form Health Survey (SF-36);Kentucky Inventory of Mindfulness Score (KIMS);Inventory of Depressive Symptomatology (IDS);adverse events; | — |
Countries
China
Contacts
Public ContactXiao-hui Wang
The First Affiliated Hospital of Jiamusi University
Outcome results
None listed