Combined TECAR/EMS Therapy vs. Standard Manual Therapy for Endometriosis Pelvic Pain
A legfontosabb adatok
- Hol
- Brooklyn (Egyesült Államok)A helyszín megnézése
Helyszínek itt: Egyesült Államok
- Inspira Physical TherapyBrooklyn, Egyesült ÁllamokContact: Melanie Carminati, PT, DPT, GTS, NCPTRésztvevőt keres
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- SWIMS America Corp.
- Azonosító
- NCT07933094
- A regiszteradat frissítve
- 2026. november 12.
- Eredeti leírás
This study compares two ways of delivering a combined radiofrequency (RET), muscle stimulation (Hi-EMS), and pulsed radiofrequency (Hi-TENS) therapy, hands-on by a physical therapist or hands-free using adhesive pads, and compares the combined therapy to hands-on manual therapy alone for pelvic pain in women with endometriosis. Participants attend 8 sessions over 6 weeks.A teljes eredeti leírásKevesebb
Comparative Effects of Combined TECAR Radiofrequency and Electrical Muscle Stimulation Therapy Versus Standard Manual Therapy for Pelvic Pain in Women With Endometriosis
This study compares two ways of delivering a combined radiofrequency (RET), muscle stimulation (Hi-EMS), and pulsed radiofrequency (Hi-TENS) therapy, hands-on by a physical therapist or hands-free using adhesive pads, and compares the combined therapy to hands-on manual therapy alone for pelvic pain in women with endometriosis. Participants attend 8 sessions over 6 weeks.
Bevonási feltételek: Women age 18 or older with a diagnosis of endometriosis (surgical/histologic or imaging-based); Pelvic pain attributable to endometriosis; Able to attend the 8-session outpatient schedule; Able to provide written informed consent.
Kizáró feltételek: Clinical concern for or diagnosis of May-Thurner syndrome with associated risk of deep vein thrombosis (DVT); Presence of a cardiac pacemaker, implantable cardioverter-defibrillator, or other active implanted electronic device; Active or suspected deep vein thrombosis or other uncontrolled clotting disorder; Open wound, active infection, or compromised skin integrity at planned electrode sites (suprapubic/lower abdominal region and sacral/gluteal region); Known malignancy in the region to be treated; Current pregnancy; Inability to tolerate electrical stimulation per participant report during device calibration.