Evaluation of a Phyto Aromatherapy Treatment in the Management of Recurrent Cystitis (CYSTALTERNA)
Primary Purpose
Cystitis Recurrent
Status
Active
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
CYSCONTROL/PHYTOCYST Herbal tea
Sponsored by
About this trial
This is an interventional treatment trial for Cystitis Recurrent
Eligibility Criteria
Inclusion Criteria:
- Women aged 18 or older.
- Affiliated to social security.
- Presenting recurrent cystitis defined by a frequency of at least 4 episodes per year.
- For women of childbearing age: effective contraception followed for at least 3 months prior to the start of the study and agreeing to keep it throughout the study period
- Available to consult a phyto-aromatherapy pharmacist for an initial consultation and then every 3 months (M3, 6,9, 12) and then at 18 months.
- Having been previously explored according to good practice and informed
- Having signed the informed consent
Exclusion Criteria:
- Pregnant or breastfeeding women
- Severe visceral deficiencies in the previous year.
- Individualised psychiatric pathology.
- Other progressive infectious pathologies requiring antibiotic treatment.
- Taking anticoagulants.
- Concomitant intake of non-drug treatments.
Sites / Locations
- Hôpital Archet
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Alternating each month for 1 year between Phytocyst herbal tea and Cyscontrol
Arm Description
Alternating each month (From Day1 to DAY15) for 1 year between Phytocyst herbal tea and Cyscontrol = Preventive Treatment In case of episode of cystitis : AROMAFEMINA, Capsules for the comfort of the urinary tract Oleocaps 2 : 2 capsules before meals, 3 times a day for 5 consecutive days.
Outcomes
Primary Outcome Measures
adherence to phyto-aromatherapy treatment
The scale called "treatment compliance" ranges from 1 to 10. A score of 1 means not at all observant and 10 means very observant.
Secondary Outcome Measures
Antibiotic treatments
The number of antibiotic treatments over 12 months
Number of cystitis
The number of cystitis over the 12 months of the protocol
Patients' overall satisfaction
Patients' overall satisfaction will be assessed on a simple numerical scale from 1 to 10. The scale is called the "General Satisfaction Scale" and ranges from 1 to 10. A score of 1 means not at all satisfied and 10 means very satisfied. As well as their ability to manage their symptoms. Three analogue scales will also be used to assess the impact of the protocol on patients' sexuality (including anxiety and comfort in relation to intercourse, when appropriate)
Recording adverse events
The nature of the side effects, sought and at each phyto-aromatherapy consultation
The benefit persisting at 6 months after stopping treatment with phyto-aromatherapy
The benefit persisting at 6 months after stopping treatment with phyto-aromatherapy will be evaluated on the number of times antibiotic therapy is used over a period of 6 months after stopping the treatment
Evaluation of the evolution of bacterial resistance on phenotypes isolated from the cytobacteriological examination of urine
Evaluation of the evolution of bacterial resistance on phenotypes isolated from the cytobacteriological examination of urine if inclusion resistance markers are present, in comparison with the last cytobacteriological examination of urine carried out during the protocol period, requested in the event of a clinical episode. A cytobacteriological examination of the urine carried out on a systematic basis that can detect asymptomatic colonisation or bacteriuria is not appropriate.
Full Information
NCT ID
NCT04747041
First Posted
February 2, 2021
Last Updated
June 22, 2023
Sponsor
Centre Hospitalier Universitaire de Nice
1. Study Identification
Unique Protocol Identification Number
NCT04747041
Brief Title
Evaluation of a Phyto Aromatherapy Treatment in the Management of Recurrent Cystitis
Acronym
CYSTALTERNA
Official Title
Evaluation of a Phyto Aromatherapy Treatment in the Management of Recurrent Cystitis Preliminary Study
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 18, 2021 (Actual)
Primary Completion Date
June 20, 2023 (Actual)
Study Completion Date
December 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Half of the women have a once-in-a-lifetime episode of cystitis. Recurrence occurs in about 20% to 30% of patients, and half of these patients will have more than 4 episodes per year, defining recurrent cystitis.
The clinical assessment sometimes brings to light favourable factors; variables in pre- or post-menopause; but in the majority of cases, no explanatory cause can solve the problem and some authors refer to resignation as a classic reaction to this problem.
several countries have already opted for alternative treatments (Nonsteroidal anti-inflammatory drugs, phytotherapy, diuresis treatment), especially since the pressure of antibiotic selection is at the root of the dramatic spread of bacterial resistances.
There is a growing interest in the potential of complementary medicine to assist in this care. Products based on cranberries, for example, have been particularly studied and a 2012 Cochrane review concluded that there is a benefit with an estimated risk reduction of between 10 and 20%. Another "alternative" approach is the use of Chinese medicinal herbs. These herbs have been used for more than 2000 years.
The implementation of phyto-aromatherapy treatment implies a global management of patients with recurrent cystitis. Initially, it involves a curative phase as soon as the first symptoms of the attack appear, thanks to a mixture of antibacterial essential oils. In a second phase, it integrates a preventive phase over several months thanks to an association of medicinal plants whose effects in this field have been proven in vitro and in vivo, allowing to rebalance a "terrain" associating anxiety, hypersensitivity to pain, a terrain willingly associated with the irritable bowel syndrome in these patients. While having few side effects, the plants will act, in the long term, at different levels: directly on the cause of the disease thanks to their antiseptic, antiadhesive and diuretic activities, but also by reducing the symptoms thanks to their anti-inflammatory, analgesic, antispasmodic and anxiolytic activities.
Investigators hypothesize that patients with recurrent cystitis can be improved by a two-phase, multi-plant, phyto-aromatherapy treatment combining several plants: the treatment of attacks, by aromatherapy, and a prophylactic treatment, by phytotherapy. In the absence of any such studies published in the literature, investigators propose a non-randomised prospective monocentric interventional pilot study on 15 patients with proof of concept and feasibility.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystitis Recurrent
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Alternating each month for 1 year between Phytocyst herbal tea and Cyscontrol
Arm Type
Experimental
Arm Description
Alternating each month (From Day1 to DAY15) for 1 year between Phytocyst herbal tea and Cyscontrol = Preventive Treatment In case of episode of cystitis : AROMAFEMINA, Capsules for the comfort of the urinary tract Oleocaps 2 : 2 capsules before meals, 3 times a day for 5 consecutive days.
Intervention Type
Combination Product
Intervention Name(s)
CYSCONTROL/PHYTOCYST Herbal tea
Intervention Description
Alternating every month from Day1 to Day15 cyscontrol and phytocyst herbal tea to prevent episode of cystitis
Primary Outcome Measure Information:
Title
adherence to phyto-aromatherapy treatment
Description
The scale called "treatment compliance" ranges from 1 to 10. A score of 1 means not at all observant and 10 means very observant.
Time Frame
12th month
Secondary Outcome Measure Information:
Title
Antibiotic treatments
Description
The number of antibiotic treatments over 12 months
Time Frame
12 months
Title
Number of cystitis
Description
The number of cystitis over the 12 months of the protocol
Time Frame
12 months
Title
Patients' overall satisfaction
Description
Patients' overall satisfaction will be assessed on a simple numerical scale from 1 to 10. The scale is called the "General Satisfaction Scale" and ranges from 1 to 10. A score of 1 means not at all satisfied and 10 means very satisfied. As well as their ability to manage their symptoms. Three analogue scales will also be used to assess the impact of the protocol on patients' sexuality (including anxiety and comfort in relation to intercourse, when appropriate)
Time Frame
12 months
Title
Recording adverse events
Description
The nature of the side effects, sought and at each phyto-aromatherapy consultation
Time Frame
18 months
Title
The benefit persisting at 6 months after stopping treatment with phyto-aromatherapy
Description
The benefit persisting at 6 months after stopping treatment with phyto-aromatherapy will be evaluated on the number of times antibiotic therapy is used over a period of 6 months after stopping the treatment
Time Frame
During 6 months after stopping treatment (patient stop treatment at Month12 so between the 12th and 18th month)
Title
Evaluation of the evolution of bacterial resistance on phenotypes isolated from the cytobacteriological examination of urine
Description
Evaluation of the evolution of bacterial resistance on phenotypes isolated from the cytobacteriological examination of urine if inclusion resistance markers are present, in comparison with the last cytobacteriological examination of urine carried out during the protocol period, requested in the event of a clinical episode. A cytobacteriological examination of the urine carried out on a systematic basis that can detect asymptomatic colonisation or bacteriuria is not appropriate.
Time Frame
From date of inclusion until the date of documented episode of cystitis, assessed up to 18 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women aged 18 or older.
Affiliated to social security.
Presenting recurrent cystitis defined by a frequency of at least 4 episodes per year.
For women of childbearing age: effective contraception followed for at least 3 months prior to the start of the study and agreeing to keep it throughout the study period
Available to consult a phyto-aromatherapy pharmacist for an initial consultation and then every 3 months (M3, 6,9, 12) and then at 18 months.
Having been previously explored according to good practice and informed
Having signed the informed consent
Exclusion Criteria:
Pregnant or breastfeeding women
Severe visceral deficiencies in the previous year.
Individualised psychiatric pathology.
Other progressive infectious pathologies requiring antibiotic treatment.
Taking anticoagulants.
Concomitant intake of non-drug treatments.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Veronique MONDAIN
Organizational Affiliation
Centre Hospitalier Universitaire de Nice
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Archet
City
Nice
ZIP/Postal Code
06202
Country
France
12. IPD Sharing Statement
Learn more about this trial
Evaluation of a Phyto Aromatherapy Treatment in the Management of Recurrent Cystitis
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