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Tranexamic Acid and Spontaneous Chronic Urticaria (TACUS)

Primary Purpose

Chronic Spontaneous Urticaria

Status
Unknown status
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
association of levocetirizine and tranexamic acid
Levocetirizine only
Sponsored by
University Hospital, Grenoble
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Spontaneous Urticaria

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with spontaneous chronic urticaria, according to the criteria of the European Academy of Allergology and Clinical Immunology (EAACI) in agreement with the European Dermatology Forum (EDF), and the World Allergy Organization (WAO), corresponding to an association of the following symptoms : urticarial eruptions and / or recurrent angioedema for at least 6 weeks

Exclusion Criteria:

  • Urticaria associated with a specific systemic disease including cutaneous and systemic mastocytosis, urticarial vasculitis, autoinflammatory diseases associated with cryopyrin
  • Bradykinin angioedema and isolated angioedema whose origin is not clearly attributable to spontaneous chronic urticaria.
  • Presence of a contraindication to tranexamic acid and to levocetirizine

Sites / Locations

  • CHU Grenoble-AlpesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Association drugs

one drug

Arm Description

levocetirizine 10mg/day + tranexamic acid (AT) 2g/day for a month

Levocetirizine 20 mg/day for a month

Outcomes

Primary Outcome Measures

Evolution of the Urticaria Activity Score 7 (UAS7)
Evolution of the UAS7 score between the beginning (J0) and the end (J28) of the treatment period. To calculate the score, the patient rates the number of papules and itching intensity from 0 to 3 daily for 7 days. 0 corresponds to no papules and no itching, 3 corresponds to more than 50 papules per 24h and intense itching that can cause daily life. This makes a score of 0 to 6 per day accumulated over 7 days, ranging from 0 to 42.
Tolerance of the association tranexamic acid and levocetirizine
Number of adverse events

Secondary Outcome Measures

To demonstrate the non-inferiority of levocetirizine 10mg / day + tranexamic acid (AT) 2g / day versus levocetirizine alone 20mg / day in terms of efficacy on the Angioedema Activity Score (AAS)
Evolution of the AAS score between the beginning (J0) and the end (J28) of the end of treatment. The AAS score is a The AAS consists of 5 questions as well as an opening question. A score between 0 and 3 is assigned to every answer field. The question scores are summed up to an AAS day sum score, 7 AAS day sum scores to an AAS week sum score (AAS7). Accordingly, the minimum and maximum possible AAS scores are 0-15 (AAS day sum score), 0-105 (AAS7).
Clinical characteristics of responders
Identify the clinical characteristics of responders to the combination rather than antihistamines alone.

Full Information

First Posted
October 17, 2018
Last Updated
April 27, 2021
Sponsor
University Hospital, Grenoble
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1. Study Identification

Unique Protocol Identification Number
NCT03789422
Brief Title
Tranexamic Acid and Spontaneous Chronic Urticaria
Acronym
TACUS
Official Title
Efficacy and Safety of Levocetirizine Alone or in Combination With Tranexamic Acid in the Treatment of Spontaneous Chronic Urticaria. Multicentric Controlled Randomized Study in Cross-over, Double-blind
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 10, 2019 (Actual)
Primary Completion Date
September 2022 (Anticipated)
Study Completion Date
September 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble

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
Spontaneous chronic urticaria (UCS) is a disease that affects 1% of the general population with a potentially severe impact on quality of life. Most patients respond favorably to long-term antihistamine treatment, but sometimes it is necessary to give a high dose (4 times the formal dose, Berlin consensus 2016). These high doses are often accompanied by side effects requiring cessation of treatment. The therapeutic alternative is then omalizumab, an expensive biotherapy. UCS is secondary to non-specific mast cell activation. It has been shown to be associated with activation of fibrinolysis that correlates with the severity of symptoms. Patients with UCS resistant to levocetirizine were shown to have higher D-dimer levels than patients who responded to antihistamines. Tranexamic acid is a molecule with antifibrinolytic propertiesSeveral cases of severe chronic urticaria responding favorably to treatment with tranexamic acid have been reported. In our department, Investigators also noticed the improvement of some of their patients on tranexamic acid. The combination of these two treatments appears to be synergistic: action on histamine receptors and control of fibrinolysis. The investigators propose to evaluate the association of tranexamic acid and levocetirizine for the treatment of chronic spontaneous urticaria.
Detailed Description
Multicentric controlled randomized crossover study, double-blind To evaluate the efficacy and safety of levocetirizine 10mg / day + tranexamic acid (AT) 2g / day versus levocetirizine 20mg / day alone in the chronic treatment of chronic urticaria evaluated at 4 weeks. A hierarchical analysis will be implemented in the following order: Non-inferiority of the combination levocetirizine 10 mg / day + tranexamic acid (TA) 2 g / day versus levocetirizine alone 20 mg / day in terms of effectiveness Superiority of the combination levocetirizine 10 mg / day + tranexamic acid (AT) 2 g / day versus levocetirizine alone 20 mg / day in terms of tolerance Superiority of levocetirizine 10mg / day + tranexamic acid (AT) 2g / day versus levocetirizine alone 20mg / day in terms of effectiveness Each objective will be tested sequentially if and only if the previous objective is validated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Spontaneous Urticaria

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
Multicentric controlled randomized crossover study, double-blind
Masking
ParticipantInvestigator
Masking Description
Double blind
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Association drugs
Arm Type
Active Comparator
Arm Description
levocetirizine 10mg/day + tranexamic acid (AT) 2g/day for a month
Arm Title
one drug
Arm Type
Active Comparator
Arm Description
Levocetirizine 20 mg/day for a month
Intervention Type
Drug
Intervention Name(s)
association of levocetirizine and tranexamic acid
Intervention Description
levocetirizine 10 mg/day + tranexamic acid 2 g/day
Intervention Type
Drug
Intervention Name(s)
Levocetirizine only
Intervention Description
levocetirizine 20 mg/day
Primary Outcome Measure Information:
Title
Evolution of the Urticaria Activity Score 7 (UAS7)
Description
Evolution of the UAS7 score between the beginning (J0) and the end (J28) of the treatment period. To calculate the score, the patient rates the number of papules and itching intensity from 0 to 3 daily for 7 days. 0 corresponds to no papules and no itching, 3 corresponds to more than 50 papules per 24h and intense itching that can cause daily life. This makes a score of 0 to 6 per day accumulated over 7 days, ranging from 0 to 42.
Time Frame
28 days
Title
Tolerance of the association tranexamic acid and levocetirizine
Description
Number of adverse events
Time Frame
28 days
Secondary Outcome Measure Information:
Title
To demonstrate the non-inferiority of levocetirizine 10mg / day + tranexamic acid (AT) 2g / day versus levocetirizine alone 20mg / day in terms of efficacy on the Angioedema Activity Score (AAS)
Description
Evolution of the AAS score between the beginning (J0) and the end (J28) of the end of treatment. The AAS score is a The AAS consists of 5 questions as well as an opening question. A score between 0 and 3 is assigned to every answer field. The question scores are summed up to an AAS day sum score, 7 AAS day sum scores to an AAS week sum score (AAS7). Accordingly, the minimum and maximum possible AAS scores are 0-15 (AAS day sum score), 0-105 (AAS7).
Time Frame
28 days
Title
Clinical characteristics of responders
Description
Identify the clinical characteristics of responders to the combination rather than antihistamines alone.
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with spontaneous chronic urticaria, according to the criteria of the European Academy of Allergology and Clinical Immunology (EAACI) in agreement with the European Dermatology Forum (EDF), and the World Allergy Organization (WAO), corresponding to an association of the following symptoms : urticarial eruptions and / or recurrent angioedema for at least 6 weeks Exclusion Criteria: Urticaria associated with a specific systemic disease including cutaneous and systemic mastocytosis, urticarial vasculitis, autoinflammatory diseases associated with cryopyrin Bradykinin angioedema and isolated angioedema whose origin is not clearly attributable to spontaneous chronic urticaria. Presence of a contraindication to tranexamic acid and to levocetirizine
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Raouf ZOUGLECH, MDS
Phone
4 76 76 78 38
Ext
0033
Email
rzouglech@chu-grenoble.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Tiphaine Montagnon
Phone
4 76 76 68 14
Ext
0033
Email
tmontagnon@chu-grenoble.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laurence BOUILLET, PhD
Organizational Affiliation
Internal Medicine - University Hospital Grenoble-Alpes
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Grenoble-Alpes
City
Grenoble
ZIP/Postal Code
38043
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mélanie Arnaud
Phone
4 76 76 78 38
Ext
0033
First Name & Middle Initial & Last Name & Degree
Laurence BOUILLET, PhD

12. IPD Sharing Statement

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Tranexamic Acid and Spontaneous Chronic Urticaria

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