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Acupuncture for Sedation in the Intensive Care Unit (ICU)

Primary Purpose

Delirium, Respiratory Depression, Overmedication

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Verum Acupuncture
Sham Acupuncture
Sponsored by
Oregon Health and Science University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Delirium focused on measuring Anxiolytics, Sedatives, Acupuncture Therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Trauma patient ≥ 18 years admitted to the Trauma ICU
  • Injury Severity Score (ISS) ≥ 4
  • Mechanically ventilated < 24 hours with anticipated need > 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

Sites / Locations

  • Oregon Health & Science University (OHSU)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Verum Acupuncture

Sham acupuncture

Arm Description

Subjects will receive acupuncture using real acupuncture needles.

Subjects will receive sham acupuncture therapy using the Streitberger needle at the same points and on the same schedule as patients in the treatment group. Streitberger needles are blunt tipped and retract into themselves rather than penetrating the skin.

Outcomes

Primary Outcome Measures

Success of Blinding
Care team, family and subject will be surveyed to determine success of blinding. Responses will be tallied and correlated with group assignments.

Secondary Outcome Measures

Richmond Agitation-Sedation Scale (RAAS) Score
Measure of sedation. Scale -5 to +4, with -5 equal to 'Unarousable' and +4 equal to 'Combative.'
Length of Ventilator Dependence
Number of hours of ventilator use

Full Information

First Posted
May 25, 2011
Last Updated
March 19, 2020
Sponsor
Oregon Health and Science University
Collaborators
Medical Research Foundation, Oregon
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1. Study Identification

Unique Protocol Identification Number
NCT01362270
Brief Title
Acupuncture for Sedation in the Intensive Care Unit (ICU)
Official Title
Acupuncture for Sedation in the Intensive Care Unit
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oregon Health and Science University
Collaborators
Medical Research Foundation, Oregon

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium, Respiratory Depression, Overmedication
Keywords
Anxiolytics, Sedatives, Acupuncture Therapy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Verum Acupuncture
Arm Type
Experimental
Arm Description
Subjects will receive acupuncture using real acupuncture needles.
Arm Title
Sham acupuncture
Arm Type
Sham Comparator
Arm Description
Subjects will receive sham acupuncture therapy using the Streitberger needle at the same points and on the same schedule as patients in the treatment group. Streitberger needles are blunt tipped and retract into themselves rather than penetrating the skin.
Intervention Type
Device
Intervention Name(s)
Verum Acupuncture
Other Intervention Name(s)
Special No. 16 needles (Gauge 8 x 1.2")
Intervention Description
DOSAGE: 25 acupoints per session FREQUENCY: 2 sessions per day DURATION: 5 days
Intervention Type
Device
Intervention Name(s)
Sham Acupuncture
Other Intervention Name(s)
Streitberger Placebo-needles (Gauge 8 x 1.2")
Intervention Description
DOSAGE: 25 acupoints per session FREQUENCY: 2 sessions per day DURATION: 5 days
Primary Outcome Measure Information:
Title
Success of Blinding
Description
Care team, family and subject will be surveyed to determine success of blinding. Responses will be tallied and correlated with group assignments.
Time Frame
Nurse surveyed daily for length of study (five [5] days). Physician and subject (or subject's family if he/she is unable to complete the questionnaire) surveyed upon study completion, six (6) days after enrollment.
Secondary Outcome Measure Information:
Title
Richmond Agitation-Sedation Scale (RAAS) Score
Description
Measure of sedation. Scale -5 to +4, with -5 equal to 'Unarousable' and +4 equal to 'Combative.'
Time Frame
Median RAAS score during treatment (5 days)
Title
Length of Ventilator Dependence
Description
Number of hours of ventilator use
Time Frame
Number hourss subject is ventilated. Subjects are expected to be ventilator dependent an average of 120 hours. Assessed up to discharge (estimated 3 weeks).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Trauma patient ≥ 18 years admitted to the Trauma ICU Injury Severity Score (ISS) ≥ 4 Mechanically ventilated < 24 hours with anticipated need > 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer M Watters, MD
Organizational Affiliation
Oregon Health and Science University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oregon Health & Science University (OHSU)
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11818761
Citation
Greif R, Laciny S, Mokhtarani M, Doufas AG, Bakhshandeh M, Dorfer L, Sessler DI. Transcutaneous electrical stimulation of an auricular acupuncture point decreases anesthetic requirement. Anesthesiology. 2002 Feb;96(2):306-12. doi: 10.1097/00000542-200202000-00014.
Results Reference
background
PubMed Identifier
11159266
Citation
Wang SM, Kain ZN. Auricular acupuncture: a potential treatment for anxiety. Anesth Analg. 2001 Feb;92(2):548-53. doi: 10.1097/00000539-200102000-00049.
Results Reference
background
PubMed Identifier
18356793
Citation
Nayak S, Wenstone R, Jones A, Nolan J, Strong A, Carson J. Surface electrostimulation of acupuncture points for sedation of critically ill patients in the intensive care unit--a pilot study. Acupunct Med. 2008 Mar;26(1):1-7. doi: 10.1136/aim.26.1.1.
Results Reference
background
PubMed Identifier
17641566
Citation
McManus CA, Schnyer RN, Kong J, Nguyen LT, Hyun Nam B, Goldman R, Stason WB, Kaptchuk TJ. Sham acupuncture devices--practical advice for researchers. Acupunct Med. 2007 Jun;25(1-2):36-40. doi: 10.1136/aim.25.1-2.36.
Results Reference
background
PubMed Identifier
18090028
Citation
Shapiro MB, West MA, Nathens AB, Harbrecht BG, Moore FA, Bankey PE, Freeman B, Johnson JL, McKinley BA, Minei JP, Moore EE, Maier RV; Inflammation and the Host Response to Injury Large Scale Collaborative Research Project. V. Guidelines for sedation and analgesia during mechanical ventilation general overview. J Trauma. 2007 Oct;63(4):945-50. doi: 10.1097/TA.0b013e318142d21b. No abstract available.
Results Reference
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Acupuncture for Sedation in the Intensive Care Unit (ICU)

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