Hysteroscopic Cryomyolysis for the Treatment of Submucosal Leiomyomata

Uterine Fibroids Clinical Trial

Official title:

Feasibility Study of Hysteroscopic Cryoablation Treatment of Symptomatic Uterine Fibroids in Women Who do Not Desire Further Pregnancies

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00731341
• Other study ID #: UFHYS_WH_ 121207 VER 0.1
• Status: Completed
• Phase: N/A
• Start date: July 2008
• Est. completion date: February 2009

Study information

• Verified date: July 2021
• Source: Boston Scientific Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the current study is to evaluate the technical success, safety and procedure feasibility of hysteroscopic cryoablation treatment of symptomatic uterine fibroids in women who do not desire further pregnancies using Galil Medical's 17-gauge 400mm Argon-based cryoablation needles

Description:

Currently there are no optimal methods for treating symptomatic uterine fibroids. Existing therapeutic options are conservative (medications), invasive (e.g., hysterectomy, surgical myomectomy), or minimally invasive (uterine artery embolization, or myolysis).

Fibroid ablation using cryogenic energy, known as Cryoablation, offers a potential alternative method of fibroid treatment. Cryotherapy is a well-established technique for the treatment of various benign and malignant conditions. Cryoablation has been described for the treatment of prostate cancer, renal cell carcinoma, liver tumors and benign and malignant breast tumors.

Galil Medical's proposed feasibility study is looking to examine the technical success, safety and feasibility of a hysteroscopic approach for the treatment of symptomatic fibroids. This technique involves the insertion and placement of Galil Medical's 17-gauge cryoablation needle(s)guided by a hysteroscopic device. Ultrasound provides real-time monitoring of the needle insertion, placement and iceball propagation during the cryoablation procedure.

This treatment offers the patient to preserve her uterus by a minimally invasive procedure. The type of the fibroids intended for treatment (Type II submucous myomas)are often very difficult to completely and safely remove hysteroscopically and are often treated through an open or laparoscopic procedure. A hysteroscopic procedure does not involve intraperitoneal intervention and is therefore expected to be associated with less intra-operative and post-operative complications.

The recovery from hysteroscopic cryoablation is expected to be fast with only minimal self resolving discomfort. The patient should be able to return to her normal activity within 24-48 hours.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3
• Est. completion date: February 2009
• Est. primary completion date: February 2009
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 30 Years to 50 Years

Eligibility

Inclusion Criteria:

• Primary complaint is excessive bleeding

• Subject is able to understand and give informed consent for participation in the study

• Pre-menopausal woman between the ages of 30 and 50 (inclusive)

• Has completed childbearing and not contemplating future fertility

• Has symptomatic uterine fibroids

• Fibroids type, size, location and number

• 1 submucosal fibroid

• Type I and Type II fibroids

• 2 to 4cm

• Using contraception to prevent pregnancy

Exclusion Criteria:

• Any evidence of known or suspected infection or pre-malignancy/malignancy

• Desire for future child bearing

• Fibroids

• Size > 4cm

• 2 or more submucosal fibroids

• Fibroid distance from the serosa is less than 1 cm

Related Conditions & MeSH terms

• Leiomyoma
• Menorrhagia
• Uterine Fibroids

Intervention

Procedure:
• Cryoablation for the treatment of uterine fibroids
Needle will be inserted into the fibroid via the cervix through a hysteroscope channel. Gas is circulated through the sealed needle to form an iceball at the tip. After insertion, the needle will be cooled to a temperature of below -100°C to freeze the tissue of the fibroid.

Locations

Country	Name	City	State
Netherlands	St.Lucas Andreas Ziekenhuis	Amsterdam

Sponsors (1)

Lead Sponsor	Collaborator
Boston Scientific Corporation

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Adverse Events	Safety of the procedure will be assessed by incidence and severity of intra and post procedure related adverse events (AEs)	up to 4 weeks post procedure.
Secondary	Hysteroscopic Cryoablation Related Pain Will be Measured by Self Reported Pain Severity Visual Analogue Scale (VAS) Completed by the Patient	Hysteroscopic cryoablation related pain will be measured by self reported pain severity Visual Analogue Scale (VAS) from a scale of 1 (no pain) to 10 (very severe pain) completed by the patient	Prior to hospital discharge (less than 24 hours post-procedure)
Secondary	Time (in Days) to Return to Normal Activity	The number of days needed to return to normal activity was assessed by the participant and reported to the investigator. The response was documented at follow-up.	4 weeks post procedure
Secondary	Number of Participants Discharged on Day of Cryoablation Procedure.	Per the protocol, this outcome intended to report the average duration of post operative hospital stay. However, this measurement was made very generally and was not collected in number of hours, only the dates were collected. The only actual data that can be stated is that all subjects were discharged from the hospital on the same day as the procedure. In order to report the average length of hospital stay, the wording on the outcome measure title has been changed.	Post procedure
Secondary	Evaluation of Length of an Average Cryoablation Procedure	Evaluation of length of an average cryoablation procedure for the treatment of uterine fibroids	Post procedure
Secondary	Physician's Satisfaction From the Ease and Convenience of the Cryoablation Procedure	Physician's satisfaction from the ease and convenience of the cryoablation procedure using a scale of 1 (very satisfied) to 5 (very dissatisfied).	Post procedure