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Completed Phase 2 Interventional Results available

A Trial of a Botanical Drug Containing East Indian Sandalwood Oil (EISO) for Treatment of Common Warts

ClinicalTrials.gov ID: NCT01286441

Public ClinicalTrials.gov record NCT01286441. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 9:24 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Multi-center, Placebo-controlled, Dose-ranging, Efficacy and Safety Trial of a New Botanical Drug Product Containing East Indian Sandalwood Oil (EISO) for Treatment of Common Warts (Verruca Vulgaris)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Nonclinical studies have shown sandalwood oil to have anti-inflammatory, anti-fungal, antiviral, and anti-bacterial activities. Previous clinical studies have shown East Indian Sandalwood oil to be promising as a treatment for common warts in adults and children. The primary objective of this study is to evaluate the efficacy and safety of 10%, 20%, and 30% East Indian Sandalwood Oil (EISO) ointment compared with the ointment placebo administered twice daily (bid) for 12 weeks for the treatment of common warts (Verruca vulgaris).

Study identification

NCT ID
NCT01286441
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
ViroXis Corporation
Industry
Enrollment
183 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2012 (Type not available)
Primary completion
Apr 2014 (Actual)
Completion
Jun 2014 (Actual)
Last update posted
May 29, 2019

2012 – 2014

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Not listed Rogers Arkansas 72758 —
Not listed Fremont California 95438 —
Not listed Lomita California 90717 —
Not listed Miami Florida 33135 —
Not listed Arlington Heights Illinois 60005 —
Not listed Elwood Indiana 46036 —
Not listed Owensboro Kentucky 42303 —
Not listed Beverly Massachusetts 01915 —
Not listed Haverhill Massachusetts 01830 —
Not listed Fort Gratiot Michigan 48059 —
Not listed Newington New Hampshire 03801 —
Not listed Portsmouth New Hampshire 03801 —
Not listed Rochester New York 14623 —
Not listed Raleigh North Carolina 27612 —
Not listed Salisbury North Carolina 28144 —
Not listed Columbus Ohio 43231 —
Not listed College Station Texas 77845 —
Not listed Dallas Texas 75234 —
Not listed San Antonio Texas 78258 —
Not listed Virginia Beach Virginia 23455 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01286441, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 29, 2019 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01286441 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →