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The purpose of this study is to evaluate device safety and effectiveness of the Eximis CS System.
Full description
This is a prospective, multi-center, single-arm study to confirm device safety and effectiveness when utilized for containment, segmentation, and extraction of uterine tissue in pre-menopausal women undergoing laparoscopic hysterectomy or myomectomy for non-cancer indications.
Eligible subjects who have signed an informed consent form (ICF) will be enrolled. Subjects will be sequentially enrolled and assigned a study identification number. Surgeons will also be assigned a unique number.
Subjects will undergo the standard of care regarding all aspects of the pre-operative, surgical, and follow-up procedures. The aspect unique to this study is the capture, segmentation, and extraction of the target tissue will utilize one integrated device, the Eximis CS System, which segments tissue via segmenting wires using RF energy. The device is not intended to provide any therapeutic effect.
All subjects will be followed for safety through a post-procedure follow-up visit that will occur at minimum 30 days and maximum 45 days post-operatively through the post-procedure follow-up visit.
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Inclusion criteria
Planned laparoscopic hysterectomy or myomectomy. Tissue specimen size is greater than 6 cm in diameter, less than 13 cm in the longest dimension, and at most 10 cm in the second longest dimension, based on preoperative assessment.
Pre-operative evaluation, which may include imaging, cervical cancer screening, and endometrial biopsy has been completed.
Signed informed consent. Willing to adhere to protocol requirements and complete follow-up.
Exclusion criteria
Subject is post-menopausal, defined as amenorrhea >12 months in the absence of ovulation suppression.
Known or suspected malignancy of gynecological origin as determined by standard clinical practice.
Candidate for en bloc tissue removal, for example through the vagina or via a mini-laparotomy incision.
Hemoglobin < 8 g/dl within 30 days prior to surgery. Subject has a current history of undiagnosed genital bleeding Subject has an implanted electronic device where use of radiofrequency (RF) energy would be contraindicated (e.g., pacemaker, internal defibrillator).
Medical condition, surgical history, or intra-operative findings, which in the option of the investigator, precludes utilization of the Eximis CS System.
Known allergy to polyurethane, polyethylene, thermoplastic fluoropolymer and/or chlorinated polyvinyl chloride.
Concurrent participation in another therapeutic or interventional clinical trial with investigational pharmaceutical agent(s) or medical device(s) that could impact evaluation of this study as determined by the Investigator.
Inability to comply with the study procedures or follow-up in the opinion of the investigator.
Subject is pregnant.
Intraoperative Exclusion: Abdominal wall thickness at the umbilicus incision site exceeds 6 cm.
Primary purpose
Allocation
Interventional model
Masking
30 participants in 1 patient group
There are currently no registered sites for this trial.
Central trial contact
Hilary A Baldwin
Start date
Sep 20, 2024 • 7 months ago
Today
Apr 29, 2025
End date
May 30, 2025 • in 1 month
Data sourced from clinicaltrials.gov
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