Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00826397 · ClinicalTrials.gov registry record · NA

Acupuncture for Aromatase Inhibitor Induced Joint Pain

A NA study, sponsored by Columbia University.

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT00826397 is a NA study that has completed, run by Columbia University. The registered enrollment target is 40 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00826397, a NA study, has completed, sponsored by Columbia University.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

This is a randomized, controlled, pilot study to determine the safety and efficacy of acupuncture as an adjunct to pharmacological treatment compared to pharmacological intervention alone for the treatment of musculoskeletal pain related to aromatase inhibitors (AI) in postmenopausal breast cancer patients. Twenty participants (20 in each arm) will be enrolled at the Breast Oncology clinic at Columbia University Medical Center (CUMC). Patients in the treatment arm will receive acupuncture administered twice weekly for six weeks and will be allowed to take pain medication as necessary. The control patients will initially receive pain medication alone, then will cross-over to the acupuncture arm after six weeks. The investigators hypothesize that acupuncture will reduce AI induced joint symptoms. The study will enroll a total of 40 patients, half of whom will be randomized to one of the two arms to receive acupuncture plus pharmacological treatment (arm A) or pharmacological treatment alone (arm B). Joint pain will be assessed by the BPI-SF score at baseline and six weeks. All patients will have a baseline BPI worst pain item (#2) ≥3 points on a scale of 0-10.

Interventions

  • PROCEDURE Acupuncture
  • PROCEDURE Sham Acupuncture

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2005-06
Est. Completion 2009-09
Phase NA

Sponsor

Columbia University

958 total trials

What the Registry Record Tells You About NCT00826397

The ClinicalTrials.gov registry entry for NCT00826397 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Acupuncture is the first listed.

NCT00826397 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00826397 about?

NCT00826397 is a clinical study titled "Acupuncture for Aromatase Inhibitor Induced Joint Pain". This is a randomized, controlled, pilot study to determine the safety and efficacy of acupuncture as an adjunct to pharmacological treatment compared to pharmacological intervention alone for the treatment of musculoskeletal pain related to aromatase inhibitors (AI) in postmenopausal breast cancer p...

What is the current status of trial NCT00826397?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2005-06. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00826397?

The interventions under investigation include: Acupuncture (PROCEDURE), Sham Acupuncture (PROCEDURE).

Who is sponsoring clinical trial NCT00826397?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.