Comparison of Boric Acid vs. Terconazole in Treatment of RVVC

NCT ID: NCT04208555

Last Updated: 2019-12-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

76 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-15

Study Completion Date

2021-05-31

Brief Summary

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Vulvovaginal candidiasis (VVC) caused by Candida species, predominantly C. Albicans is considered one of the most common infections of the lower female genital tract affecting 75% of women at least once in their lifetime. Recurrent VVC (RVVC) is arbitrarily defined as four or more episodes every year. RVVC is a debilitating, long-term condition that can severely affect the quality of life of women. Several factors have been associated with RVVC such as prolonged use of antibiotics, inadequately treated infection, uncontrolled diabetes, immune mechanisms (e.g. HIV), oral contraceptive use as well as the resistance of non-albicans Candida species (e.g. C glabrata, C krusei) to conventional antifungal agents as azoles.

Fluconazole administered orally is the most commonly used antifungal drug in the case of RVVC. However, in the last decade, fluconazole-resistant C Albicans has been reported in women with RVVC. Terconazole is a broad-spectrum, triazole antifungal treatment agent for both C Albicans and non-albicans. Its use (80 mg vaginal suppository daily for 6 days) was as effective as two doses of oral fluconazole (150 mg) in the treatment of patients with severe VVC and RVVC.

Boric acid or boracic \[B(OH)3\] is a weak acid with proven antifungal action. In RVVC especially in azole-resistant strains and in non-Candida Albicans, 600 mg of the boric acid vaginal suppository is recommended once daily for 2 weeks. This regimen has a mycologic cure rate varied from 40% to 100%. However, there are no published studies comparing the intravaginal use of boric acid with terconazole for RVVC. Accordingly, a prospective randomized study in patients with RVVC will be conducted to address this important issue.

Detailed Description

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Conditions

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Vulvovaginal Candidiasis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Boric acid vaginal suppository

Group Type EXPERIMENTAL

Boric Acid Vaginal Suppository

Intervention Type DRUG

Boric acid vaginal suppository (600 mg/day) for 14 days

Terconazole vaginal suppository

Group Type ACTIVE_COMPARATOR

Terconazole Vaginal Suppository

Intervention Type DRUG

Terconazole 80 mg vaginal suppository daily for 6 days

Interventions

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Boric Acid Vaginal Suppository

Boric acid vaginal suppository (600 mg/day) for 14 days

Intervention Type DRUG

Terconazole Vaginal Suppository

Terconazole 80 mg vaginal suppository daily for 6 days

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of RVVC will be defined as four or more episodes of VVC that occurred during the previous 12-month period.
* Has symptoms and signs of VVC e.g. itching, burning, discharge, and erythema.
* Documented VVC on high vaginal swabs (HVSs) by the demonstration of blastospores and pseudohyphae in a wet vaginal smear treated with 10% potassium hydroxide, and a positive fungal culture.
* Age: 18-50 years old and premenopausal.
* Agree to abstain from sexual intercourse during the treatment period.
* Agree to abstain from using any other vaginal product during the study period.

Exclusion Criteria

* Postmenopausal.
* Pregnancy.
* Sexually transmitted infection (Chlamydia, gonorrhea, trichomonas).
* Any antifungal or antibiotic use 14 days prior to treatment.
* Gynecological conditions requiring treatment e.g. Bartholin's cyst, abscess, PID.
* Patients receiving corticosteroids or immunosuppressive therapy.
* Patients expected to menstruate within seven days of the start of treatment.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hatem AbuHashim

OTHER

Sponsor Role lead

Responsible Party

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Hatem AbuHashim

Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Hatem Abu Hashim, MD. FRCOG. PhD

Role: STUDY_CHAIR

Faculty of Medicine, Mansoura University

Asmaa Swidan, MBBCh

Role: PRINCIPAL_INVESTIGATOR

New Mansoura General Hospital

Central Contacts

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Hatem Abu Hashim, MD.FRCOG.PhD

Role: CONTACT

Phone: +20502300002

Email: [email protected]

References

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Iavazzo C, Gkegkes ID, Zarkada IM, Falagas ME. Boric acid for recurrent vulvovaginal candidiasis: the clinical evidence. J Womens Health (Larchmt). 2011 Aug;20(8):1245-55. doi: 10.1089/jwh.2010.2708. Epub 2011 Jul 20.

Reference Type BACKGROUND
PMID: 21774671 (View on PubMed)

Other Identifiers

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MS.19.09.825

Identifier Type: -

Identifier Source: org_study_id