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Completed Phase 2 Interventional Results available

Minocycline Hydrochloride in Reducing Chemotherapy-Induced Peripheral Neuropathy and Acute Pain in Patients With Breast Cancer Undergoing Treatment With Paclitaxel

ClinicalTrials.gov ID: NCT02297412

Public ClinicalTrials.gov record NCT02297412. 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 27, 2026, 5:16 PM EDT

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

Official title

Pilot Clinical Trial Evaluating the Utility of Minocycline as an Agent to Decrease Chemotherapy-Induced Peripheral Neuropathy (CIPN) and Paclitaxel-Induced Acute Pain Syndrome (P-APS): A Randomized Placebo-Controlled, Double Blind Trial

Brief summary

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

This randomized pilot trial studies how well minocycline hydrochloride works in reducing chemotherapy-induced peripheral neuropathy and acute pain in patients with breast cancer undergoing treatment with paclitaxel. Drugs used in chemotherapy, such as paclitaxel, may cause damage to nerves that result in aches, pains, and tingling or numbness of fingers and toes. Minocycline hydrochloride may help lessen nerve damage from paclitaxel and improve the quality of life in breast cancer patients.

Study identification

NCT ID
NCT02297412
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
47 participants

Conditions and interventions

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 2014 (Type not available)
Primary completion
Jul 8, 2016 (Actual)
Completion
Jul 8, 2016 (Actual)
Last update posted
Jan 31, 2022

2014 – 2016

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
PCR Oncology Pismo Beach California 93449 —
Illinois CancerCare-Community Cancer Center Normal Illinois 61761 —
Carle Cancer Center Urbana Illinois 61801 —
Siouxland Regional Cancer Center Sioux City Iowa 51101 —
Michigan Cancer Research Consortium NCORP Ann Arbor Michigan 48106 —
Mayo Clinic Rochester Minnesota 55905 —
Coborn Cancer Center at Saint Cloud Hospital Saint Cloud Minnesota 56303 —
Missouri Valley Cancer Consortium Omaha Nebraska 68106 —
Hematology Oncology Associates of Central New York-East Syracuse East Syracuse New York 13057 —
Novant Health Oncology Specialists Winston-Salem North Carolina 27103 —
Women and Infants Hospital Providence Rhode Island 02905 —
Marshfield Clinic Marshfield Wisconsin 54449 —

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 NCT02297412, 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 Jan 31, 2022 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02297412 live on ClinicalTrials.gov.

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