Tailored Radiofrequency Ablation of Uterine Myomas

Sponsor
International Evangelical Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04091529
Collaborator
(none)
54
1
1
25
2.2

Study Details

Study Description

Brief Summary

To perform the use of radiofrequency myolysis (RFM) for the treatment of intra-uterine fibroids through less invasive access by combining trans-vaginal ultrasound, hysteroscopy and laparoscopy

Condition or Disease Intervention/Treatment Phase
  • Device: RADIOFREQUENCY ABLATION OF UTERINE MYOMAS
N/A

Detailed Description

Given that the RF ablation of solid tumors of the liver and other organs is successfully used as a usual approach, the investigators have decided to transfer this technology to an original treatment of uterine fibroids. The access to each individual fibroid was determined considering passage of the needle towards its centre through only compromised tissue and by the shortest possible route by combining trans-vaginal ultrasound, hysteroscopy and laparoscopy. To optimize radiofrequency myolysis, in fact, the investigators decided to improve the procedure by inserting three innovative elements: application of a virtual needle tracking system to follow the RF electrode during the ablation session, real-time monitoring of RF ablation by contrast-enhanced ultrasound and systematic biopsy of the lesions before electro-coagulation.

Study Design

Study Type:
Interventional
Actual Enrollment :
54 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Prospective Study on Radiofrequency Ablation of Uterine Fibroids (Myolysis) Under Ultrasound and Endoscopic Guidance, in Single or Combined Approach
Actual Study Start Date :
Mar 1, 2017
Actual Primary Completion Date :
Mar 1, 2019
Actual Study Completion Date :
Mar 31, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Radiofrequency myolysis of uterine fibroids

54 premenopausal participants with symptomatic uterine myomas

Device: RADIOFREQUENCY ABLATION OF UTERINE MYOMAS
The ablation device consisted of an radiofrequency (RF) energy generator (STARmed, RF generator VRS01) and an electric pump for the continuous cooling of the electrode tip. The RF generator to which the electrode (STARmed Gyeonggi-Do, Korea) is connected displays simultaneously the temperature of the electrode tip, the tissue impedance characteristics, the power and the ablation time. A 35 cm long 18Gauge internally cooled electrode with an exposed tip of 10 mm or a variable exposed tip was used
Other Names:
  • Radiofrequency myolysis (RFM)
  • RF lesion generator for tissue ablation during surgical procedures. Sterile single-use RF coagulation monopolar electrode.
  • Outcome Measures

    Primary Outcome Measures

    1. Myoma volumes after radiofrequency myolysis (RFM) [12 months]

      The outcomes evaluated after RFM were myoma volumes (cubic centimeters)

    2. Myoma diameters after radiofrequency myolysis (RFM) [12 months]

      The outcomes evaluated after RFM were myoma diameters (centimeters)

    3. Uterine Fibroid Symptom and Quality of Life (UFS-QOL) score after radiofrequency myolysis (RFM) [12 months]

      Uterine Fibroid Symptom and Quality of Life (UFS-QOL) questionnaire with scores ranging from 0 to 100, were higher QOL scores mean a better health-related QOL 1 and a 10-point scale used for each reported symptom.

    Secondary Outcome Measures

    1. Surgical time of radiofrequency myolysis (RFM) [12 months]

      The surgical time (minutes) for each different type of surgical access

    2. Surgical time of radiofrequency myolysis (RFM) assisted by new technologies [12 months]

      The reduction of surgical time (minutes) with the use of a virtual global positioning system (GPS) track system or a contrast-enhanced ultrasound during the ablation

    3. Pre-intervention biopsy associated to radiofrequency myolysis (RFM) [12 months]

      The number of biopsies for treated fibroma

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 62 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes

    "Inclusion Criteria":

    • women who had symptomatic myomas with diameters ranging between 1.2 and 7.7 cm. - patients who had declined hysterectomy or laparoscopic myomectomy

    • submucosal fibroids with intramural extension ≥50%

    • intramural fibroids (FIGO G3 / G4 types)

    • subserosal fibroids (FIGO G5 / G6 types)

    "Exclusion Criteria":

    • Women with intracavitary (FIGO G0 / G1 types) or subserosal-pedunculated fibroids / (FIGO G7 types)

    • genital malignancy

    • cervical dysplasias

    • pelvic infection / adhesions

    • severe systemic diseases

    • pregnancy

    • deeply infiltrating endometriosis

    • patients who took gonadotropin-releasing hormone therapy or acetate ulipristal within 6 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 International Evangelical Hospital Genoa Italy 16125

    Sponsors and Collaborators

    • International Evangelical Hospital

    Investigators

    • Principal Investigator: Alessandro FASCIANI, International Evangelical Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Alessandro FASCIANI, MD - Principal Investigator, International Evangelical Hospital
    ClinicalTrials.gov Identifier:
    NCT04091529
    Other Study ID Numbers:
    • 295/2018
    First Posted:
    Sep 16, 2019
    Last Update Posted:
    Sep 18, 2019
    Last Verified:
    Sep 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 18, 2019