Effectiveness of Low-dose Naltrexone in Patients With Different Types of Vulvodynia
Launched by MEDICAL UNIVERSITY OF LUBLIN · Jul 12, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the effectiveness of a medication called low-dose naltrexone (LDN) in women who experience vulvodynia, a condition characterized by chronic pain in the vulvar area. The researchers want to see if LDN can help reduce pain and improve the quality of life for women suffering from different types of this condition. To participate, women must be between 18 and 50 years old, have a diagnosis of vulvodynia, and be in generally good health. They also need to agree to use effective contraception during the study.
Participants in the trial will be randomly assigned to either receive LDN or a placebo (a pill that looks the same but has no active medication) for comparison. The study is designed to ensure that neither the participants nor the researchers know who is receiving which treatment, which helps to keep the results unbiased. If you are considering joining, you can expect to have regular check-ins to monitor your health and any changes in your pain levels throughout the study. This trial is important because it may help identify new treatment options for vulvodynia, a condition that currently has limited standard treatments.
Gender
FEMALE
Eligibility criteria
- 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.
About Medical University Of Lublin
The Medical University of Lublin is a distinguished academic institution dedicated to advancing healthcare through innovative research and clinical trials. With a strong emphasis on interdisciplinary collaboration, the university fosters a vibrant environment for medical and scientific inquiry, aiming to improve patient outcomes and contribute to the broader medical community. Its commitment to ethical research practices and patient safety ensures that all clinical trials conducted under its auspices adhere to the highest standards of scientific rigor and regulatory compliance. The Medical University of Lublin is positioned at the forefront of medical education and research in Poland, making significant contributions to the fields of medicine, pharmacy, and health sciences.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lublin, , Poland
Patients applied
Trial Officials
Ewa Baszak-Radomańska, MD, PhD
Principal Investigator
Terpa Limited Liability Company Limited partnership
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported