EVADRY® in the Treatment of Xerostomia in Sjögren's Syndrome — DRYLESS  

Sjogren's Syndrome Clinical Trial

Official title: DRYLESS: Randomized Controlled Trial of EVADRY® vs Placebo in the Treatment of Xerostomia in Sjögren's Syndrome

Status Not yet recruiting

Clinical Trial Summary

Xerostomia is a common and very bothersome manifestation that impairs the quality of life in Sjogren's syndrome. Symptomatic therapeutic alternatives for this syndrome are limited in Tunisia. We resort to bromhexine off-label with low efficacy. The aim of this work is to demonstrate the superiority of a treatment based on dietary supplements (EVADRY) vs placebo in the treatment of xerostomia. This is a double-blind randomized clinical trial with 2 arms: an EVADRY arm (n=90) and a placebo arm (n=90). The primary outcome measure is a 35% increase in salivary flow after 3 months. Secondary outcome measures were based on the Oral Health Impact Profile questionnaire, Xerostomia Inventory, the HAD depression scale, and the buccal Schirmer test.

Clinical Trial Description

Study design: This is a randomized controlled double-blind clinical trial involving 2 groups: - Group 1: consisting of 90 patients receiving the EVADRY dietary supplement treatment. - Group 2: consisting of 90 patients receiving a placebo Inclusion and exclusion criteria: • Inclusion criteria: The included patients meet the following criteria: - age over 18 years - diagnosis of Sjogren's syndrome according to ACR/EULAR 2016 criteria - continuous xerostomia for more than 3 months - initial salivary flow rate < 0.1 ml/min • Non-inclusion criteria: - allergy or hypersensitivity to any of the products - pregnancy - breastfeeding - oral or throat surgery before wound healing - cognitive or dementia disorders - Exclusion criteria: These include: - Occurrence of cognitive or dementia disorders - Pregnancy - Allergy to any of the components of the EVADRY product - Indication of oral or throat surgery Randomization: This is a randomization by random blocks. A co-investigator (who is not in contact with the patients) will be responsible for this randomization. The EVADRY treatment and the placebo will have the same packaging. Codes will be assigned to the sprays by the investigator responsible for the randomization. These codes will be placed in sealed envelopes and will only be opened at the end of the study. They will be kept by another investigator who has no knowledge of the randomization. Treatment and interventions: The EVADRY oral spray and the placebo are produced by Wellnet laboratory. • EVADRY spray: It is a phytotherapy-based medication in the form of an oral spray. It is a 100 ml bottle containing ALEO BARBADENSIS LEAF WATER (1 ml), Chamomilla Recutita Flower extract (30 mg), TOCOPHEROL (10 mg), hyaluronic acid (2 mg), mentha spicata herb oil (10 mg), and eugenol (40 µg). - The placebo corresponds to flavored water (mint extract) with the same taste as EVADRY. It is placed in a bottle with the same appearance as EVADRY. Both products are administered at a rate of 5 intra-oral sprays per day. Evaluation criteria: • Primary evaluation criterion: It is based on the measurement of salivary flow rate (SFR). It consists of asking the patient to collect their saliva in the morning without prior stimulation (no smoking, chewing gum, or alcohol one hour before) in a graduated tube for 15 minutes. The patient should be comfortably seated with their head slightly tilted forward and their mouth open to allow saliva to flow. A value less than 0.1 ml/minute corresponds to hyposalivation. • Secondary evaluation criteria: - Xerostomia Inventory in French version: it is a questionnaire composed of 11 questions. For each item, there is an evaluation of its frequency (never, rarely, occasionally, quite often, very often). The total score ranges from 11 to 55 points. - OHIP-14 questionnaire: it includes 7 dimensions with 14 items to assess quality of life. The higher the score on this questionnaire, the more negative the impact on quality of life. - HAD scale: it is an instrument that allows screening for anxiety and depressive disorders. It consists of 14 items rated from 0 to 3 : 7 for anxiety and 7 for depression. We will have 2 scores. A score ≤7 corresponds to the absence of symptoms, ≥11 corresponds to definite symptomatology, and between the two, it is doubtful. - Buccal Schirmer test: it consists of a strip of Whatman paper (blotting paper) placed in a polyethylene bag, with the first 5 mm of the strip protruding from one end of the bag. This end is then folded and placed under the patient's tongue in contact with the floor of the mouth for 5 minutes. The patient should be in a forward-leaning position, hands on knees, and eyes closed. After five minutes, the strip is removed and the soaked portion is measured in centimeters. Patient follow-up: The patients will be interviewed and examined initially. During this consultation, the patient's epidemiological and clinical data will be collected. During the same consultation, SFR and buccal Schirmer test will be measured, and Xerostomia Inventory, OHIP-14, and HAD will be calculated. These tests will be repeated at 1, 2, and 3 months. Interruption and end of the trial: Patient follow-up is planned for 3 months. The statistical study is planned for 1 month. ;

Related Conditions & MeSH terms

• Sjogren's Syndrome
• Syndrome
• Xerostomia

• NCT number: NCT06313905
• Study type: Interventional
• Source: University Tunis El Manar
• Contact: Fatma Saïd
• Phone: 0021671150876
• Email: saidzribifatma@yahoo.fr
• Status: Not yet recruiting
• Phase: N/A
• Start date: April 15, 2024
• Completion date: December 31, 2025