Effectiveness of Low-dose Naltrexone in Patients With Different Types of Vulvodynia

Quality of Life Clinical Trial

Official title:

Effectiveness of Low-doses of Naltrexone (LDN) on Pain Perception and Quality of Life in Women With Vulvodynia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05955313
• Other study ID #: VN21
• Status: Recruiting
• Phase: Phase 2
• Start date: May 31, 2023
• Est. completion date: December 31, 2026

Study information

• Verified date: July 2023
• Source: Medical University of Lublin
• Contact: Andrzej Stepulak, Professor
• Phone: 448 52 98
• Email: cwnr[@]umlub.pl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: December 31, 2026
• Est. primary completion date: December 31, 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

1. Women from the age of 18 to the menopause or to the age of 50 (on the day of inclusion for testing).

2. Patients who are not pregnant and do not plan to become pregnant in the next 9 months from the inclusion in the study

3. Signing the patient's informed and voluntary consent to participate in the study.

4. General health of the patient (WHO = 0-2).

5. Diagnosis of vulvodynia.

6. Negative drug test found at the visit randomization.

7. Documented correct cytology result from 3 years ago (before the visit screening).

8. Stable dose of drugs acting on the central nervous system used min. 1 month before the screening visit and during the entire patient's participation in the study.

9. Acceptance or readiness to use a highly effective method of contraception from the screening visit throughout the study. Sexual abstinence is not accepted.

10. The ability to understand the principles of testing and operating electronic devices.

Exclusion Criteria:

1. Severe, hepatic and renal dysfunction defined as:

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.

2. Abuse of alcohol (more than 14 units per week) and other stimulants. 3. Taking psychoactive substances, including drugs, except for SSRI, SNRI, SARI (Trazodone), and anticonvulsants (Gabapentin, Pregabalin, Lamotrigine) in fixed doses from the screening visit.

4. Taking opioid drugs in the last 2 months before the screening visit (also in OTC preparations, eg Loperamide).

5. Taking naltrexone hydrochloride and Mysimba for weight loss at any time in your life.

6. BTA injection in the vulva in the last 4 months before the screening visit. 7. Endovascular procedures in the area of the small pelvis in the last 6 months before the screening visit.

8. Previous surgical procedures requiring general anesthesia (with general anesthesia) in the last 2 months before the screening visit.

9. Completed multidisciplinary therapeutic program in the treatment of vulvodynia in the last 4 months before the screening visit.

10. Diseases of the vulva: lichen, current contact vulvovaginitis, bacterial and / or yeast infections, other dermatological diseases, recurrent genital herpes (HSV; min 4 times / year).

11. Diagnosis of current or past serious mental disorders according to the criteria of ICD-10 and DSM-5, including psychotic and organic disorders (except depression and anxiety disorders).

12. Gynecological abnormalities requiring medical treatment: current HSIL, CIN II / III, pelvic inflammation, mixed or solid ovarian tumors, simple ovarian cysts greater than 5 cm, abnormal vaginal inter-cycle bleeding.

13. Pelvic venous diseases (PeVD), 4 criteria met on USG. 14. Pregnancy and lactation. 15. Spastic diseases: multiple sclerosis (MS), connective tissue diseases (Marfan syndrome and marfan-like syndromes), reactive arthritis (RA). 16. Vaginismus, Lamont scale 3-5 (gynecological examination impossible due to anxiety).

17. Significant and / or uncorrected disability in the field of sight or hearing, making it difficult to perform psychological tests.

Related Conditions & MeSH terms

• Naltrexone
• Quality of Life
• Vulvodynia

Intervention

Drug:
• Naltrexone Hydrochloride
treatment of vulvodynia

Locations

Country	Name	City	State
Poland	Terpa Limited Liability Company Limited Partnership	Lublin

Sponsors (1)

Lead Sponsor	Collaborator
Medical University of Lublin

Country where clinical trial is conducted

Poland, 

References & Publications (1)

Baszak-Radomanska E, Wanczyk-Baszak J, Paszkowski T. Pilot study of testing a clinical tool for pelvic physical examination in patients with vulvodynia. Ginekol Pol. 2021 Mar 23. doi: 10.5603/GP.a2020.0168. Online ahead of print. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Treatment effectiveness - change in pain intensity	measured by 11-point NRS scale based on spontaneously experienced vulvar and vaginal pain and during vaginal penetration	from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
Primary	Treatment effectiveness - change in type and severity of pain	measured by McGill Questionnaire (SF-MPQ)	from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
Primary	Treatment effectiveness - change in emotional functioning	Beck Depression Inventory (BDI-II)	from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
Primary	Patient's satisfaction	measured by 11-point Lickert scale	from pre-treatment values (VISIT 2) to end of treatment values (VISIT 4) assessed for 4 months
Secondary	Treatment tolerability	Assessment of the tolerability of LDN therapy based on the assessment of side effects and adverse events	throughout the treatment period (from VISIT 2 to VISIT 4) assessed for 4 months