ClinicalTrials.gov record
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 May 20, 2026, 8:53 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

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

Study identification

NCT ID
NCT02297412
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Academic and Community Cancer Research United
Other
Enrollment
47 participants

Conditions and interventions

Interventions

  • Minocycline Hydrochloride Drug
  • Placebo Other
  • Quality-of-Life Assessment Other
  • Questionnaire Administration Other

Drug · Other

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
Oct 31, 2014
Primary completion
Jul 7, 2016
Completion
Jul 7, 2016
Last update posted
Jan 30, 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 30, 2022 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02297412 live on ClinicalTrials.gov.

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