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Effects of Microcrystalline Titanium Dioxide With Covalently Linked Monovalent Silver Ions on Complications After Total Hysterectomy (ISTIAB-1)

Primary Purpose

Infection, Bleeding, Complication, Postoperative

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
TIAB: microcrystalline titanium dioxide with covalently linked monovalent silver ions
Placebo
Sponsored by
Università degli Studi dell'Insubria
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Women underwent laparoscopic total hysterectomy for benign gynecological pathology

Exclusion Criteria:

  • Women underwent non-laparoscopic total hysterectomy
  • Women underwent laparoscopic total hysterectomy for malignant pathology
  • Patients with diabetes mellitus in insulin therapy
  • Smoking patients
  • Patients suffering from chronic rheumatic diseases or chronic diseases not in adequate control.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    TIAB treatment

    Placebo

    Arm Description

    From the first postoperative day for ten days, single vaginal capsule per day of TIAB (microcrystalline titanium dioxide with covalently linked monovalent silver ions), Sodium Hyaluronate, and Aloe Barbadensis Extract vaginal capsule.

    From the first postoperative day for ten days, single vaginal capsule per day of sodium Hyaluronate, and Aloe Barbadensis Extract vaginal capsule.

    Outcomes

    Primary Outcome Measures

    Vaginal bleeding
    at least one episode of red vaginal blood loss
    Vaginal vault infection
    at least one episode of inflammation and infection in the vaginal vault suture requiring antibiotic therapy
    Urinary tract infection
    at least one episode of signs and symptoms requiring empiric antibiotic therapy
    Dehiscence of vaginal vault suture
    Dehiscence of vaginal vault suture requiring repeat surgery
    Readmission
    At least one episode of readmission related to postoperative complications

    Secondary Outcome Measures

    Adverse events
    Adverse events due to the use of vaginal capsule therapy: erythema, vaginal and vulvar pruritus, dermatitis.

    Full Information

    First Posted
    December 27, 2018
    Last Updated
    December 28, 2018
    Sponsor
    Università degli Studi dell'Insubria
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03789799
    Brief Title
    Effects of Microcrystalline Titanium Dioxide With Covalently Linked Monovalent Silver Ions on Complications After Total Hysterectomy
    Acronym
    ISTIAB-1
    Official Title
    Randomized Controlled Trial on the Use of Microcrystalline Titanium Dioxide With Covalently Linked Monovalent Silver Ions (TIAB) in the Formulation of Vaginal Capsules in the Prevention of Complications After Total Hysterectomy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 1, 2019 (Anticipated)
    Primary Completion Date
    June 30, 2019 (Anticipated)
    Study Completion Date
    December 31, 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Università degli Studi dell'Insubria

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Total hysterectomy is one of the most performed surgical procedures in the world and it is associated with post-operative complications. The postoperative morbidity rate is estimated to vary from 3% to 8% with a readmission rate of 5-7%. The most frequent postoperative complications are urinary tract infections, wound infection of the vaginal vault, vault cellulitis, bleeding, suture dehiscence, pelvic abscess. The introduction of routine antibiotic prophylaxis has significantly reduced the risk of infectious complications, which however remains higher than other "clean" surgery, mainly due to contamination by the vaginal bacterial flora. In this scenario, the introduction of adjuvant factors acting on bacterial flora, can contribute to reduce the risk of post-surgical complications. The cationic silver ions (Ag +) stabilized by covalent link with Titanium dioxide (TiO2), the TIAB, maximizes the properties of silver by optimizing the antibiotic action and disruptive properties of the pathogenic biofilm of bacteria and fungi. Thanks to these properties, TIAB is able to enhance the antibiotic action by reducing the risk of antibiotic resistance and recurrent infections linked to the biofilm. Re-establishing the optimal vaginal microenvironment represents a fundamental step reducing the risk of infections in the surgical site, since the vagina is a non-sterile environment populated by bacterial species that can generate biofilm and potentially infect the site of surgery. In addition to microbicidal and disruptive biofilm activity, TIAB has demonstrated a direct action on tissue regeneration processes by stimulating the production of collagen and its modeling. Different clinical trials have reported a cicatrizing and re-epithelializing action of TIAB administered vaginally in the context of cervical conization for pathology related to HPV. Without showing any notable adverse effects or a negative action on lactobacillary flora with an overall good therapy tolerance by patients. On the basis of the available evidence, we conduct a randomized controlled clinical trial to determine if TIAB treatment in the formulation of vaginal capsules TIAGIN (TIAB (microcrystalline titanium dioxide with covalently linked monovalent silver ions), Sodium Hyaluronate, Aloe Barbadensis Extract) is able to reduce the incidence of infectious complications, that are related to altered healing of post-hysterectomy vaginal suture.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Infection, Bleeding, Complication, Postoperative

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomized controlled double-blind trial
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Masking Description
    TIAGIN and placebo will be provided in identical non-distinguishable packaging and formulations. To each pack a unique random ID will be assigned based on an independently generated random scheme (www.randomization.com). Patients will blindly receive consecutively a single pack of 10 vaginal capsules. The same blinding procedure will also be present for health professionals (double-blind study) as only the manufacturer will be aware of the contents of the pack. For each enrolled patient, the patient ID will be associated to the packaging ID, the maintenance of the confidentiality of such data will be the responsibility of the Principal Investigator, to which the contents of the pack will be revealed only at the end of the study for the final data analysis.
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    TIAB treatment
    Arm Type
    Experimental
    Arm Description
    From the first postoperative day for ten days, single vaginal capsule per day of TIAB (microcrystalline titanium dioxide with covalently linked monovalent silver ions), Sodium Hyaluronate, and Aloe Barbadensis Extract vaginal capsule.
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    From the first postoperative day for ten days, single vaginal capsule per day of sodium Hyaluronate, and Aloe Barbadensis Extract vaginal capsule.
    Intervention Type
    Other
    Intervention Name(s)
    TIAB: microcrystalline titanium dioxide with covalently linked monovalent silver ions
    Intervention Description
    TIAGIN vaginal capsule, composition: TIAB (microcrystalline titanium dioxide with covalently linked monovalent silver ions), Sodium Hyaluronate, Aloe Barbadensis Extract
    Intervention Type
    Other
    Intervention Name(s)
    Placebo
    Intervention Description
    Placebo vaginal capsule, composition: Sodium Hyaluronate, Aloe Barbadensis Extract
    Primary Outcome Measure Information:
    Title
    Vaginal bleeding
    Description
    at least one episode of red vaginal blood loss
    Time Frame
    Between the 10th post operative day and the 30th post operative day
    Title
    Vaginal vault infection
    Description
    at least one episode of inflammation and infection in the vaginal vault suture requiring antibiotic therapy
    Time Frame
    Between the first post operative day and the 30th post operative day
    Title
    Urinary tract infection
    Description
    at least one episode of signs and symptoms requiring empiric antibiotic therapy
    Time Frame
    Between the 10th post operative day and the 30th post operative day
    Title
    Dehiscence of vaginal vault suture
    Description
    Dehiscence of vaginal vault suture requiring repeat surgery
    Time Frame
    Between the 10th post operative day and the 30th post operative day
    Title
    Readmission
    Description
    At least one episode of readmission related to postoperative complications
    Time Frame
    Between the day of discharge and the 30th post operative day
    Secondary Outcome Measure Information:
    Title
    Adverse events
    Description
    Adverse events due to the use of vaginal capsule therapy: erythema, vaginal and vulvar pruritus, dermatitis.
    Time Frame
    Between the first post operative day and the 30th post operative day

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Women underwent laparoscopic total hysterectomy for benign gynecological pathology Exclusion Criteria: Women underwent non-laparoscopic total hysterectomy Women underwent laparoscopic total hysterectomy for malignant pathology Patients with diabetes mellitus in insulin therapy Smoking patients Patients suffering from chronic rheumatic diseases or chronic diseases not in adequate control.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Simone Garzon, M.D.
    Phone
    +39 347 0782287
    Email
    sgarzon@studenti.uninsubria.it
    First Name & Middle Initial & Last Name or Official Title & Degree
    Antonio Simone Laganà, M.D.
    Phone
    ‭+39 329 6279579‬
    Email
    antoniosimone.lagana@asst-settelaghi.it
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Simone Garzon, M.D.
    Organizational Affiliation
    Università degli Studi dell'Insubria
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Antonio Simone Laganà, M.D.
    Organizational Affiliation
    Università degli Studi dell'Insubria
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Fabio Ghezzi, M.D.
    Organizational Affiliation
    Università degli Studi dell'Insubria
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Jvan Casarin, M.D.
    Organizational Affiliation
    Università degli Studi dell'Insubria
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Effects of Microcrystalline Titanium Dioxide With Covalently Linked Monovalent Silver Ions on Complications After Total Hysterectomy

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