Terpa Limited Liability Company Limited Partnership
Lublin, 20-333, Poland
Location status: Recruiting
NCT Number: NCT05955313
Vulvodynia (Vd) is chronic functional vulvar pain, with prevalence of 3-16% and unclear etiopathology. Although Vd significantly deteriorates quality of life, the problem is marginalized, no pharmacologic treatment standards exist. Naltrexone hydrochloride is a specific opioid antagonist with slight agonist activity. There is growing body of evidence supporting the effectiveness of low-dose naltrexone (LDN) in different types of chronic pain. The main goal of this trial is to test the effect of LDN on pain perception and quality of life in women with different types of Vd. Half of the study population receives LDN and the remaining patients take placebo, according to randomization list. This RTC is quadruplet blinded.
Interested in participating?
Request Info18 year–50 year
Female
Interventional
Phase 2
Lublin, 20-333, Poland
Location status: Recruiting
In this Randomized Controlled Trial the effectiveness of LDN in reducing chronic pain and improvement of quality of life in women with provoked, spontaneous or mixed vulvodynia is assessed on the basis of the test results recommended according to IMMPACT protocol, compared to the placebo arm. Patients remain in the study for 6 months (4 months of treatment with LDN or placebo). There are 5 visits by a gynecologist (diagnosis of vulvodynia, inclusion and exclusion criteria, randomization), nurse, psychologist and physiotherapist: screening, randomization, control telephone visit, final visit and telephone summary visit. Pain perception and quality of life estimation is reported by the patient in e-diary, validated psychology questionnaires are fulfilled and physical examination acc. Fascial Manipulation (CFMS) L. Stecco method is performed. Tolerability of LDN therapy will also be assessed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
i. An ASPT or ALT result 5 times the upper limit; ii. The level of bilirubin 3 times above the upper limit of normal - excluding patients with Gilbert's syndrome; iii. EGFR result below 30 ml / min / m2, on the basis of historical studies not older than 3 years before the screening visit or from the tests performed during the screening visit according with point 12 of the Protocol, version 1.0 of March 28, 2022.
treatment of vulvodynia
Other names: naltrexone
Time frame: from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
measured by 11-point NRS scale based on spontaneously experienced vulvar and vaginal pain and during vaginal penetration
Time frame: from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
measured by McGill Questionnaire (SF-MPQ)
Time frame: from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
Beck Depression Inventory (BDI-II)
Time frame: from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
measured by 11-point Lickert scale
Time frame: throughout the treatment period (from VISIT 2 to VISIT 4) assessed for 4 months
Assessment of the tolerability of LDN therapy based on the assessment of side effects and adverse events
Contact information is provided by the study sponsor or research team.
Medical University of Lublin
Other
Effectiveness of Low-doses of Naltrexone (LDN) on Pain Perception and Quality of Life in Women With Vulvodynia
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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