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MODUCARE Versus Wait-and-See Approach for Histologically Proven Low-grade Cervical Intraepithelial Neoplasia (CIN1)

A Randomized Trial of MODUCARE Versus Wait-and-See Approach for Histologically Proven Low-grade Cervical Intraepithelial Neoplasia (CIN1)

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07379905
Acronym
MODUCIN1
Enrollment
182
Registered
2026-02-02
Start date
2026-03-01
Completion date
2028-03-01
Last updated
2026-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low-grade Cervical Intraepithelial Neoplasia, Moducare

Brief summary

MODUCIN-1 (MODUcare for CIN1) is a prospective, single center, open-label, randomized trial that its purpose is to compare MODUCARE versus Wait-and-See Approach for the regression rate of histologically proven low-grade Cervical Intraepithelial Neoplasia (CIN1).

Detailed description

Human Papillomavirus (HPV) is causally associated with cervical cancer and precancerous lesions (dysplasias) of the cervix. These lesions are detected mainly in the transformation zone and are diagnosed with colposcopy and biopsy confirmation. In high-grade lesions conization (surgical removal of a cone tissue form the cervix) is the therapy of choice, but in low-grade lesions monitoring and no-treatment is preferred. However, this wait-and-see approach can be assisted by pharmaceutical treatment, like MODUCARE. MODUCARE is classified as a natural dietary supplement, specifically an immune support supplement containing a patented blend of plant sterols and sterolins, primarily beta-sitosterol and beta-sitosterol glucoside, derived from plant sources. It is taken orally, 2 capsules three times daily for the first month and then 1 capsule three times daily for next 5 months (in total 6 months).

Interventions

DIETARY_SUPPLEMENTMODUCARE

MODUCARE is classified as a natural dietary supplement, specifically an immune support supplement containing a patented blend of plant sterols and sterolins, primarily beta-sitosterol and beta-sitosterol glucoside, derived from plant sources.

Sponsors

Aristotle University Of Thessaloniki
Lead SponsorOTHER
INPA S.A.
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

* ARM A: Control Arm for Wait-and-See approach * ARM B: Intervation Arm for MODUCARE oral capsules, dosage 2 x 3 for 1 month and 1 x 3 for 5 months (total 6 months, as per instructions provided by the manufacturer)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Histologically proven CIN1 * Any HPV status (negative, positive: high or low risk) * Any Pap test result * Age 18 - 85 years old * ECOG Performance status 0 - 1

Exclusion criteria

* Pregnancy * Low likelihood of patient compliance to treatment protocol and follow-up * Previous operation to the cervix * Previous pelvic malignancy * Pre-existing histologically proven CIN1 \> 12 months * Pre-existing histologically proven CIN2 and/or CIN3 * Hypersensitivity to trial medication

Design outcomes

Primary

MeasureTime frame
Regression rate of CIN16 months after randomization

Secondary

MeasureTime frame
Regression rate of CIN112 months after randomization
Progression rate of CIN16 & 12 months after randomization
Treatment related adverse events: 6 months after randomization

Contacts

CONTACTDimitrios Zouzoulas, MD, MSc, PhD
dzouzoulas@hotmail.gr+306946536065
PRINCIPAL_INVESTIGATORDimitrios Tsolakidis, Dr.Prof.

Aristotle University Of Thessaloniki

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 15, 2026