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Evaluation of a Phyto Aromatherapy Treatment in the Management of Recurrent Cystitis

Evaluation of a Phyto Aromatherapy Treatment in the Management of Recurrent Cystitis Preliminary Study

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04747041
Acronym
CYSTALTERNA
Enrollment
15
Registered
2021-02-10
Start date
2021-05-18
Completion date
2026-01-23
Last updated
2025-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystitis Recurrent

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.

Interventions

COMBINATION_PRODUCTCYSCONTROL/PHYTOCYST Herbal tea

Alternating every month from Day1 to Day15 cyscontrol and phytocyst herbal tea to prevent episode of cystitis

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
adherence to phyto-aromatherapy treatment12th monthThe scale called treatment compliance ranges from 1 to 10. A score of 1 means not at all observant and 10 means very observant.

Secondary

MeasureTime frameDescription
Number of cystitis12 monthsThe number of cystitis over the 12 months of the protocol
Patients' overall satisfaction12 monthsPatients' 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)
Antibiotic treatments12 monthsThe number of antibiotic treatments over 12 months
The benefit persisting at 6 months after stopping treatment with phyto-aromatherapyDuring 6 months after stopping treatment (patient stop treatment at Month12 so between the 12th and 18th month)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 urineFrom date of inclusion until the date of documented episode of cystitis, assessed up to 18 monthsEvaluation 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.
Recording adverse events18 monthsThe nature of the side effects, sought and at each phyto-aromatherapy consultation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026