EligibleTrials

Is Repetitive Transcranial Magnetic Stimulation Effective in Reducing Endometriosis-associated Pain

Recruiting · NCT06333353 · Interventional (participants receive a specific treatment) · Lead sponsor: University of Ottawa

View the official record on ClinicalTrials.gov →
Endometriosis

Interventions studied

Real RepetitiveTranscranial Magnetic Stimulation 10 sessionsReal RepetitiveTranscranial Magnetic Stimulation 5 sessionsSham RepetitiveTranscranial Magnetic Stimulation 10 sessionsSham RepetitiveTranscranial Magnetic Stimulation 5 sessions

What this trial is about

The goal of this research is to improve pain outcomes for the over 500K Canadian women, girls and gender-diverse individuals who are newly diagnosed with endometriosis each year. Chronic pain that persists after interventions for endometriosis is a huge problem. There is some evidence that endometriosis-associated pain (EAP) is, at least to some extent, associated with changes in pain physiology, particularly central sensitization of pain. There is currently no effective evidence-informed intervention that addresses EAP. Yet a recent feasibility trial on a repetitive transcranial magnetic stimulation (rTMS) intervention demonstrated promising results compared to a sham intervention for reducing pain in a sample with EAP. The objectives of this trial are: 1. to evaluate the effectiveness of an rTMS intervention for pain reduction among those with recalcitrant post-operative EAP, 2. to inform on the utility of a long (10 session) vs short (5 session) protocol for pain reduction among those with recalcitrant post-operative EAP 3. to determine if any improvements in pain observed 30 days after an rTMS intervention are retained 6 months later 4. to identify physical and psychosocial mediators that impact the successful reduction of pain among patients with EAP treated using rTMS. 5. to describe patients' perceptions of and satisfaction with rTMS as an intervention for EAP.

Who can take part

Age range
18 Years to 60 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

1 location listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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