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

NCT00260494 · ClinicalTrials.gov registry record · NA

Acupuncture and Post-Surgical Wound Healing

A NA study, sponsored by University of California, San Francisco.

Terminated
Registry status
NA
Development phase
65
Enrollment target

NCT00260494: Clinical Trial NA study, sponsored by University of California, San Francisco.

NCT00260494 is a NA study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 65 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00260494, a NA study, was terminated before completion, sponsored by University of California, San Francisco.

TERMINATED
Registry status
NA
Development phase
65 participants
Enrollment target

Study Summary

The purpose of this study is to determine if acupuncture improves wound healing. Since we, the investigators at the University of California, San Francisco (UCSF), know that how much oxygen is delivered to tissue is the best predictor of how well a wound will heal, we are measuring changes in tissue oxygen of wounds before and after acupuncture treatments. We are focusing on the leg wounds of coronary artery bypass graft (CABG) patients who have their saphenous veins harvested in an open fashion since this is a fairly well controlled patient model.

Interventions

  • OTHER sham acupuncture
  • OTHER acupuncture

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2005-03
Est. Completion 2006-07
Phase NA

Why NCT00260494 stopped before completion

NCT00260494 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

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

NCT00260494 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00260494 about?

NCT00260494 is a clinical study titled "Acupuncture and Post-Surgical Wound Healing". The purpose of this study is to determine if acupuncture improves wound healing. Since we, the investigators at the University of California, San Francisco (UCSF), know that how much oxygen is delivered to tissue is the best predictor of how well a wound will heal, we are measuring changes in tissue...

What is the current status of trial NCT00260494?

This trial is currently terminated. It is a NA study. The enrollment target is 65 participants. The study started on 2005-03. Estimated completion is 2006-07.

What interventions are being tested in trial NCT00260494?

The interventions under investigation include: sham acupuncture (OTHER), acupuncture (OTHER).

Who is sponsoring clinical trial NCT00260494?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00260494's enrollment target sits among peer trials

65 1144th of 2000 higher than 854 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

  • NCT03366116 · 65 participants · Phase 1

    5-aza-4'-Thio-2'-Deoxycytidine (Aza-TdC) in People With Advanced Solid Tumors

  • NCT03603730 · 65 participants · NA

    Vagal Nerve Stimulation for Functional Dyspepsia and Gastroparesis

  • NCT03796559 · 65 participants · NA

    Magseed Enabled Long-Term Localization of Axillary Lymph Nodes

  • NCT03993106 · 65 participants · Phase 2

    A Study of sEphB4-HSA in Kaposi Sarcoma

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 NCT00260494, the US trial registry maintained by the National Library of Medicine. NCT00260494 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.