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Ear Electro-stimulation for Chronic Pelvic Pain

CompletedNot applicableNCT01345331
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The Brigham and Women's Pain Management Center is conducting a research study for chronic pelvic pain patients due to endometriosis. The study will assess the effect of electro-stimulation for the treatment of Chronic Pelvic Pain. You may be eligible if you have chronic pelvic pain due to endometriosis, are between the ages of 21- 64, and not taking opioid medication (such as morphine or oxycodone). The study will require two visits, each lasting about 2 hours. The study takes place at the Brigham \& Women's Pain Management Center, 850 Boylston St., Chestnut Hill. Please contact Chrissie Cahalan at 617-732-9014 or ccahalan1@partners.org if interested.

Study details

Official title
Ear Electro-stimulation for Chronic Pelvic Pain
Conditions
Interventions
  • Behavioral: Real stimulation VS Sham
Sponsor
Brigham and Women's Hospital
Collaborators
Massachusetts General Hospital
Start date
2009-05
Primary completion
2011-04
Sex
Female
Age range
from 21 Years to 64 Years
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Female volunteers between 21 and 64 years of age with chronic pelvic pain for more than six months by self report. Six months of chronic pain is the criteria most often used in CPP research. * CPP diagnoses will include endometriosis pain. * Average pain intensity of ≥4 on a scale from 0 to 10, because \<4 is considered a level with acceptable pain and function * At least an 8th grade English-reading level; English can be a second language provided that the subjects feel they understand all the questions used in the assessment measures. Exclusion Criteria: * Any interventional procedure for CPP two weeks prior to the study or during the two-week study period, such as lumbar epidural steroids, nerve root blocks, etc. * Any etiology for CPP due to a known local somatic lesion for the pain (e.g. fibroids etc.) documented by the patient's gynecologist, surgery and/or imaging. We wish to focus on functional CPP, which may be more amenable to RAVANS due to the systemic nature of VNS. * Opioid usage, either oral or intrathecal. * Surgical therapy in the previous 12 weeks, the intent to undergo surgery during the study period, or any clinically unstable systemic illness that is judged to interfere with the trial. * Non-ambulatory status * History of cardiac or nervous system disease that, in the investigator's judgment, precludes participation in the study because of a heightened potential for adverse outcome. * An inability to complete questionnaires accurately. * Cancer or other malignant disease, except carcinoma in situ of the skin * Pregnancy

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01345331