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Study identifier: NCT06908200 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Radiofrequency in Women With Chronic Pelvic Pain With an Associated Myofascial Syndrome Versus Myofascial Therapy and no Treatment

Condition: Chronic Pelvic Pain  ·  Sponsor: Hospital Clinic of Barcelona

PhaseNA
Planned participants80
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

A randomised clinical trial is being conducted in the Gynecology Department of the Hospital Clinic de Barcelona in women presenting chronic pelvic pain syndrome due to a myofascial cause which is over a 4 score in the VAS scale and not related to an obstetric injury. This study presents 4 groups; two groups receive 8 radiofrequency sessions, one group receives 8 sessions of myofascial release therapy (MRT) and the last group receives no treatment at all (NT). The two RF groups have been divided into a RF intervention group (RFIG) and a RF control group (RFCG) which receives sham treatment. The RF groups are double-blinded. Other than RF, both groups perform daily Thiele massage at home. The sessions last for 20 minutes and take place once a week during 8 weeks. The main variable evaluated is the level of pain during the muscular assessment carried out by an expert pelvic floor physical therapist using the Verbal numeric Scale in the first session and at the end of the 8 sessions. Secondary variables are: sexual function (throughout FSFI questionnaire), pain catastrophizing (ECD), quality of life (EQ5D), anxiety and depression (HADS), central sensitization (CSI) as well as other pelvic floor dysfunction symptoms (PFDI).

This description comes directly from the study's public registry record.

Talk to the study team

Carla Box, PT, MSc  ·  +34932275300  ·  cebox@clinic.cat

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Clinic de BarcelonaBarcelona, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06908200