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Not listed Phase 3 Interventional

CREATE-1: A Study to Assess the Efficacy and Safety of AXS-02 in Patients With CRPS-1

ClinicalTrials.gov ID: NCT02504008

Public ClinicalTrials.gov record NCT02504008. 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 21, 2026, 7:07 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

CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Oral Zoledronate) Administered Orally to Subjects With Complex Regional Pain Syndrome Type I (CRPS-I)

Brief summary

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

This is a randomized, double-blind, placebo-controlled, 24-week study to evaluate the efficacy and safety of AXS-02 in patients with CRPS-I.

Study identification

NCT ID
NCT02504008
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Axsome Therapeutics, Inc.
Industry
Enrollment
190 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
Jul 2015 (Actual)
Primary completion
Jan 2019 (Estimated)
Completion
Jan 2019 (Estimated)
Last update posted
Mar 23, 2018

2015 – 2019

United States locations

U.S. sites
29
U.S. states
17
U.S. cities
29
Facility City State ZIP Site status
Not listed Tucson Arizona — —
Not listed Hot Springs Arkansas — —
Not listed Encinitas California — —
Not listed La Jolla California — —
Not listed Los Angeles California — —
Not listed Napa California — —
Not listed Temecula California — —
Not listed Denver Colorado — —
Not listed Clermont Florida — —
Not listed Miami Florida — —
Not listed Orlando Florida 32827 —
Not listed Tampa Florida — —
Not listed West Palm Beach Florida — —
Not listed Canton Georgia — —
Not listed Marietta Georgia — —
Not listed St. Marys Georgia 31558 —
Not listed Meridian Idaho — —
Not listed Chicago Illinois — —
Not listed Louisville Kentucky — —
Not listed Albuquerque New Mexico — —
Not listed New York New York — —
Not listed Winston-Salem North Carolina — —
Not listed Oklahoma City Oklahoma — —
Not listed Portland Oregon — —
Not listed Dallas Texas — —
Not listed San Antonio Texas — —
Not listed Bellevue Washington — —
Not listed Seattle Washington — —
Not listed Madison Wisconsin — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02504008, 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 Mar 23, 2018 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02504008 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →