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
About this trial
This is an interventional treatment trial for Infection
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.
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
NCT ID
NCT03789799
First Posted
December 27, 2018
Last Updated
December 28, 2018
Sponsor
Università degli Studi dell'Insubria
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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