Prospective, interventional, single-center, longitudinal, single-arm pilot study to evaluate
pregnancies following the Acessa™ treatment of uterine myomas in women who desire future
Device: radiofrequency generator
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT03028610
Ages eligible for Study
18 Years to 40 Years
Genders eligible for Study
Accepts Healthy Volunteers
Are premenopausal and aged 18 to 40 years.
Have already consented to have their fibroids treated with the Acessa™ procedure.
Desire pregnancy within two years following Acessa™ treatment
Have a normal endometrial cavity as delineated by sonohysterogram within 6 months prior to treatment.
Have a uterine size relating to ≤14 weeks of pregnancy, as determined by palpatory pelvic exam.
Have fibroids identified by transvaginal ultrasound with:
≤6 (six) fibroids of ≤5 cm at the major diameter
a total uterine volume of no greater than 300 cc
Patients with type 2 fibroids are acceptable for inclusion.
Are current in their screening for cervical cancer precursors (i.e. PAP 1 or 2).
Are capable of providing informed consent.
Are willing and able to comply with all study tests, procedures, and assessment tools during screening and up to 3 years post treatment.
Are able to pass a pre-operative health exam (ASA I-III).
Patients who are currently undergoing fertility treatments (e.g. Clomid, IVF, etc.) or who are planning such treatments may be enrolled in the study.
Have contraindications for laparoscopic surgery and/or general anesthesia.
Have cervical myomas or Type 0 or Type 1 myomas. Type 0 and Type 1 myomas are excluded as these are generally accessible to hysteroscopic approaches. Cervical myomas are difficult to treat and present a greater risk of bladder or urethral injury.
Have one or more Type 0 (completely intracavitary) or Type 1 resectable submucous fibroids.
Have known or suspected abdominal adhesions which are expected to complicate laparoscopic surgery.
Have known or suspected untreated intra-uterine adhesions or uterine septum.
Have previously undergone endometrial ablation, uterine artery embolization, or uterine artery ligation/occlusion, high-intensity focused ultrasound, laparoscopic, hysteroscopic or abdominal myomectomy, or any other uterine-preserving technique for reduction of menstrual bleeding.
Subjects taking platelet-inhibiting drugs such as nonsteroidal anti-inflammatory drugs
(NSAIDs), aspirin, and clopidogrel
Are pregnant or lactating.
Have known or suspected severe endometriosis.
Have known or suspected adenomyosis.
Have active or history of pelvic inflammatory disease.
Have a history of or evidence of gynecologic malignancy or pre-malignancy within the past five years.
Have had pelvic radiation.
Have a persistent and undiagnosed complex adnexal mass.Are unable to give informed consent.
In the medical judgment of the investigator should not participate in the study.
All locations for NCT03028610
University Women's Hospital
Tübingen, Germany, 72076
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View full eligibility
Tris trial is registered with FDA with number: NCT03028610. The sponsor of the trial is University Women's Hospital Tübingen and it is looking for 25 volunteers for the current phase.
Official trial title: Pregnancy Outcome Following Global Fibroid Ablation Using the Acessa™ System
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