Bladder Pain Syndrome Clinical Trial
Official title:
Chronic Bladder Pain Syndrome in Women: Can Doxycycline Help? A Prospective, Randomised,Placebo-controlled, Double-blind Study
Chronic bladder pain syndrome is a chronic disabling disorder characterized by chronic pelvic pain, pressure or discomfort perceived to be related to the urinary bladder accompanied by at least one other urinary symptom such as persistent urgency or frequency in the absence of an identifiable cause. Chronic bladder pain syndrome severely decreases an individual's quality of life and represents a significant financial burden to those affected by it. Currently, multifactorial pathogenesis is assumed including endocrine-involvement, pelvic floor muscle irregularities, immunologic aspects and chemical causes. Corresponding to the wide spectrum of presumptive triggers, a large number of therapeutic approaches are propagated, however most are associated with limited effectiveness. Thus, treatment of BPS is a challenge and the ideal therapy remains to be elucidated. Microorganisms such as Chlamydia trachomatis, Ureaplasma urealyticum and Mycoplasma genitalium remains a challenge so that these organisms may well be involved in the pathogenesis of chronic bladder pain syndrome. The investigators hypothesise that doxycycline orally for 4 weeks, including therapy of the sexual partner, can significantly relieve symptoms in women with chronic bladder pain syndrome
Background
Doxycycline is used to treat bacterial infections. Doxycycline is in a class of medications
called tetracycline antibiotics. In addition to the general indications for all members of
the tetracycline antibiotics group, doxycycline is frequently used to treat chronic
prostatitis and pelvic inflammatory disease. Especially intracellular agents, such as
chlamydia, are generally susceptible to doxycycline. Assuming this infection to be
responsible for the chronic bladder pain syndrome in women, therapy will be performed in
accordance with the authorised indication and dosage.Bacterial cystitis is an exclusion
criterion for the diagnosis of chronic bladder pain syndrome. However, the detection of
microorganisms such as Chlamydia trachomatis, Ureaplasma urealyticum and Mycoplasma
genitalium remains a challenge so that these organisms may well be involved in the
pathogenesis of chronic bladder pain syndrome. This is supported by the findings of our
retrospective study1 that doxycycline orally for 4 weeks including therapy of the sexual
partner lead to a reduction of symptoms in 71% of women complaining of persistent urgency
and frequency, chronic urethral and/or bladder pain. Therefore, doxycycline therapy is
sensible, especially considering that there are only a few, costly and often little
effective symptomatic other treatment options.
Thus, we aim to investigate the effectiveness of doxycycline in women with chronic bladder
pain syndrome in a prospective, randomised, placebo-controlled, double-blind study.
Chronic bladder pain syndrome is a chronic disabling disorder characterized by chronic
pelvic pain, pressure or discomfort perceived to be related to the urinary bladder
accompanied by at least one other urinary symptom such as persistent urgency or frequency in
the absence of an identifiable cause2. In Europe, prevalence rates in women range from 306
to 450/100'0003,4 - much higher than previously estimated. Thus, chronic bladder pain
syndrome is a serious economic problem for every health care system. In addition, chronic
bladder pain syndrome severely decreases an individual's quality of life and represents a
significant financial burden to those affected by it. Currently, multifactorial pathogenesis
is assumed including endocrine-involvement, pelvic floor muscle irregularities, immunologic
aspects and chemical causes. Corresponding to the wide spectrum of presumptive triggers, a
large number of therapeutic approaches are propagated, however most are associated with
limited effectiveness. Thus, treatment of BPS is a challenge and the ideal therapy remains
to be elucidated. We hypothesise that doxycycline orally for 4 weeks, including therapy of
the sexual partner, can significantly relieve symptoms in women with chronic bladder pain
syndrome.
Objective
To proof or reject the effectiveness of doxycycline in treatment of chronic bladder pain
syndrome
Methods
This is a prospective, randomised, placebo-controlled double-blind trial. Recruitment of the
study participants is performed in the urologic outpatient clinic of University Hospital
Inselspital Bern.
The randomisation-list in the institute of pharmacy University Hospital Inselspital Bern
will only be accessible to unblinded employees. In case of unblinding an authorized member
of the blinded trial team contacts the 24-hours service-number of the pharmacist on-duty in
the institute of pharmacy. After disclosure of the patient-number, the pharmacist on-duty
performs the unblinding and informs the authorized unblinded trial-member about allocation.
Finally unblinding is registered on the randomization list by the pharmacist on-duty.
The unblinded trial-member will record the name of the person who performed unblinding and
the date and reason for unblinding in the patient's medical record.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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