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

NCT01633996 · ClinicalTrials.gov registry record · NA

Effectiveness of Acupuncture for Depressed Patients Taking Antidepressant Medications

A NA study, sponsored by Massachusetts General Hospital.

Completed
Registry status
NA
Development phase
45
Enrollment target

NCT01633996: Completed NA study, sponsored by Massachusetts General Hospital.

NCT01633996 is a NA study that has completed, run by Massachusetts General Hospital. The registered enrollment target is 45 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01633996, a NA study, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
NA
Development phase
45 participants
Enrollment target

Study Summary

In this research study, the investigators piloted a uniform acupuncture treatment protocol among adults with depression who were taking an antidepressant medication that was providing only partial or no symptom alleviation. The study's aims were evaluate the efficacy, safety, and tolerability of acupuncture augmentation treatment among this population. The investigators hypothesized that acupuncture as an augmentation treatment would be associated with a response rate of at least 50%, which the investigators defined as a decrease in depressive symptoms from the beginning to the end of the study of 50% or more, and that the response would be greater among patients who received acupuncture 2 times per week (vs. 1 time per week). The investigators also hypothesized that acupuncture would be associated with minimal side effects.

Primary Outcome

The HAM-D-17 is a clinician-rated measure of patient depressive symptoms (structured interview). Higher cumulative scores indicate more severe depression. A 50% or greater reduction in HAM-D-17 from baseline to endpoint was considered representative of our hypothesized acupuncture-augmentation response rate of at least 50%.

Interventions

  • PROCEDURE Acupuncture

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2007-08
Est. Completion 2010-04
Phase NA
Massachusetts General Hospital

2,032 total trials

What the finished NCT01633996 record still lists

NCT01633996 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Acupuncture is the first listed.

NCT01633996 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01633996 about?

NCT01633996 is a clinical study titled "Effectiveness of Acupuncture for Depressed Patients Taking Antidepressant Medications". In this research study, the investigators piloted a uniform acupuncture treatment protocol among adults with depression who were taking an antidepressant medication that was providing only partial or no symptom alleviation. The study's aims were evaluate the efficacy, safety, and tolerability of acu...

What is the current status of trial NCT01633996?

This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2007-08. Estimated completion is 2010-04.

What interventions are being tested in trial NCT01633996?

The interventions under investigation include: Acupuncture (PROCEDURE).

Who is sponsoring clinical trial NCT01633996?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01633996's enrollment target sits among peer trials

45 1411th of 2000 higher than 578 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00804154 · 45 participants · Phase 1

    Resiniferatoxin to Treat Severe Pain Associated With Advanced Cancer

  • NCT01851694 · 45 participants · NA

    Beta-cell Response to Incretin Hormones in Cystic Fibrosis

  • NCT02896335 · 45 participants · Phase 2

    Palbociclib and Pembrolizumab In Central Nervous System Metastases

  • NCT03454035 · 45 participants · Phase 1

    Ulixertinib/Palbociclib in Patients With Advanced Pancreatic and Other Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01633996, the US trial registry maintained by the National Library of Medicine. NCT01633996 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.