Condition: Endometriosis-related Pain · Sponsor: Göteborg University
The study evaluates the effect of TENS (transcutaneous electrical nerve stimulation) as add-on treatment compared with conventional analgesic treatment in patients with endometriosis-related chronic pain. Patients with frequent pain and high pain intensity will be randomized to additional treatment with TENS or conventional treatment for 8 weeks to evaluate the acute effects of TENS treatment (n=40). Patients with endometriosis-related pain that is not frequent or without high pain intensity constitute an external control group. All patients in the study will receive TENS treatment for a total of 16 weeks, for evaluation of long-term effects of TENS treatment.
This description comes directly from the study's public registry record.
Paulin Andréll, MD, PhD · +46-31-3438259 · paulin.andrell@gu.se
Cecilia Ögren, RN · +46-31-3425000 · cecilia.ogren@vgregion.se
Always discuss trial participation with your own doctor first.
| Pain Centre, Department of Anaesthesiology and Intensive Care Medicine Östra, Sahlgrenska University Hospital, Region Västra Götaland | Gothenburg, Sweden | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05152264