N/A
N=15
Acupuncture for Sedation in the Intensive Care Unit (ICU)
Delirium · Respiratory Depression · Overmedication
Bottom Line
View on ClinicalTrials.gov: NCT01362270 ↗Enrolled (actual)
15
Serious AEs
0.0%
Results posted
Mar 2020
Primary outcome: Primary: Success of Blinding — 1; 1 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Verum Acupuncture (Device); Sham Acupuncture (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Oregon Health and Science University
- Primary completion
- Jul 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Success of Blinding |
1; 1 | — |
| SECONDARY Richmond Agitation-Sedation Scale (RAAS) Score |
-1.4; -1.9 | — |
| SECONDARY Length of Ventilator Dependence |
62.1; 232.8 | — |
Summary
BACKGROUND Many patients in the trauma intensive care unit (TICU) require mechanical ventilation and sedation or anxiolysis. Mechanical ventilation means that a machine is helping a patient breathe if he can't breathe on his own. Because of the mechanical ventilation, these patients also require some medication to help keep them calm. These are called sedatives or anxiolytics.
The purpose of this study is to see if acupuncture can lower the amount of sedation and anxiolysis needed by a subject during mechanical ventilation in the TICU. Acupuncture is a medical procedure. Hair-thin sterile needles are inserted at specific points on the body.
PROCEDURES Some subjects will get acupuncture and others will get 'fake' acupuncture. By using 'fake' acupuncture, no one other than the acupuncturists will know which group a subject is in. Subjects and the team do not get to pick which subject is in which group. Instead, the groups are picked randomly. Subjects will get real or fake acupuncture twice a day for five days.
Standard of care - Both groups will receive the standard of care while in the study. They will be mechanically ventilated and given sedatives and analgesics based on the TICU protocol.
Real acupuncture group - This group will receive real acupuncture with real needles. These are stainless steel, one time use, needles. This group will also receive "ear tacks" which are like little needles that can stay on the ear for a few days. The ear tacks will be covered with a bandage so no one can tell which group the subject is in.
Sham acupuncture group - This group will receive sham needles. These needles retract into themselves much like a 'magic sword' rather than poking the skin. Subjects in this group will not get ear tacks. In order to hide the group the subject is in, a bandage will be used to cover part of the ear.
HYPOTHESIS Real acupuncture will decrease subject's sedation requirements by 30% when compared to the sham acupuncture group.
Eligibility Criteria
Inclusion Criteria
- Trauma patient ≥ 18 years admitted to the Trauma ICU
- Injury Severity Score (ISS) ≥ 4
- Mechanically ventilated 24 hours
Exclusion Criteria
- Inability to obtain consent from patient or designee
- Receiving immunosuppressive therapy
- Receiving therapeutic anticoagulant therapy
- History of bleeding disorder, INR > 1.5, PTT > 65, PLT < 20K
- Pregnancy
- Three (3) or more inaccessible acupoints
- Head injury with elevated intracranial pressure or requiring operation
- Patients with midline abdominal incision
- Non-english speaking
- Receipt of dexmedetomidine prior to or during study period
Data sourced from ClinicalTrials.gov (NCT01362270). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.