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Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermuscular Approach Total Hip Arthroplasty (Aquamantys)

Primary Purpose

Osteoarthritis, Hip, Joint Deformities, Acquired, Hip Dislocation, Congenital

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Aquamantys
standard electrocautery (Bovie)
Sponsored by
Joint Implant Surgeons, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Hip focused on measuring randomized controlled trial, Blood loss, surgical, Blood loss, postoperative, Wound healing

Eligibility Criteria

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

Inclusion Criteria:

  • Undergoing primary unilateral total hip arthroplasty via the anterior supine intermuscular approach
  • Patient is willing and able to complete all follow-up visits at 6 weeks and 1 year

Exclusion Criteria:

  • Patients with pre-existing known coagulopathy
  • Patients on chronic Coumadin (Warfarin) therapy
  • Patients receiving erythropoietin therapy for anemia

Sites / Locations

  • Joint Implant Surgeons, Inc.

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Aquamantys Malleable Bipolar Sealer

Standard Treatment

Arm Description

In 100 patients randomly assigned, primary total hip arthroplasty via an anterior supine intermuscular approach will be performed with the assistance of the Aquamantys Malleable Bipolar Sealer with Light.

100 patients randomly assigned will undergo primary total hip arthroplasty via the anterior supine intermuscular approach performed with the assistance of standard electrocautery.

Outcomes

Primary Outcome Measures

Perioperative Change in Hemoglobin Level
All patients will undergo routine lab work perioperatively. No additional studies will be necessary for this protocol. Hemoglobin level will be first measured preoperatively at the time of preadmission testing, which must be performed not more than 30 days prior to surgery, and then measured on postoperative day one. The two levels will be compared to assess the decrease in hemoglobin level resulting from the surgical intervention.
Perioperative Blood Transfusion Requirement
Perioperative blood transfusion requirements will be recorded, including transfusions administered during the surgical intervention and throughout the acute hospital stay.
Perioperative Blood Loss
Anesthesia and nursing records will be monitored for blood loss intraoperatively, and postoperatively via drain output. Drains will be pulled daily at 0600 and measured.

Secondary Outcome Measures

The development of complications in the wound, either as an inpatient or after discharge
Wound care will be evaluated by a designee who will be blinded to the randomization. Wound will be evaluated for drainage, erythema, and ecchymosis. Additionally, the wound healing will be scored as: Healing better than expected, As expected, or Worse than expected. Wound evaluations will occur each postoperative day in hospital (average 2 days), at 6 weeks, and 1 year.
Length of stay
Length of acute hospital stay will be recorded.

Full Information

First Posted
April 18, 2012
Last Updated
April 23, 2012
Sponsor
Joint Implant Surgeons, Inc.
Collaborators
Medtronic, Mount Carmel Health System
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1. Study Identification

Unique Protocol Identification Number
NCT01583465
Brief Title
Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermuscular Approach Total Hip Arthroplasty
Acronym
Aquamantys
Official Title
Open Label, Randomized, Blinded Study to Evaluate the Efficacy of Aquamantys System for Reducing the Transfusion Requirements Associated With the Anterior-Supine Intermuscular (ASI) Approach for Total Hip Arthroplasty (THA)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Joint Implant Surgeons, Inc.
Collaborators
Medtronic, Mount Carmel Health System

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to establish whether or not there is a clinical advantage to the use of Aquamantys® System from Medtronic Advanced Energy (formerly Salient Surgical Technologies) in patients undergoing primary total hip arthroplasty via the anterior supine intermuscular surgical approach in terms of blood loss, transfusion and wound healing. Wound healing will be assessed by a blinded observer and based upon a simple and subjective criteria: a) as expected, b) better than expected or c) worse than expected. The blinded observer is experienced in the care of the surgical patient and wound evaluation.
Detailed Description
To establish in a randomized, blinded study whether or not there is a clinical advantage to the use of Aquamantys® System from Medtronic Advanced Energy (formerly Salient Surgical Technologies) in patients undergoing primary total hip arthroplasty via the anterior supine intermuscular surgical approach in terms of blood loss, transfusion and wound healing based on early collected data. Data will be analyzed using StatsDirect in standard fashion to elucidate any difference between control and treatment groups. Wound healing will be assessed by a blinded observer and based upon a simple and subjective criteria: a) as expected, b) better than expected or c) worse than expected. The blinded observer is experienced in the care of the surgical patient and wound evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Hip, Joint Deformities, Acquired, Hip Dislocation, Congenital, Osteonecrosis, Arthritis, Rheumatoid
Keywords
randomized controlled trial, Blood loss, surgical, Blood loss, postoperative, Wound healing

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Aquamantys Malleable Bipolar Sealer
Arm Type
Experimental
Arm Description
In 100 patients randomly assigned, primary total hip arthroplasty via an anterior supine intermuscular approach will be performed with the assistance of the Aquamantys Malleable Bipolar Sealer with Light.
Arm Title
Standard Treatment
Arm Type
Active Comparator
Arm Description
100 patients randomly assigned will undergo primary total hip arthroplasty via the anterior supine intermuscular approach performed with the assistance of standard electrocautery.
Intervention Type
Device
Intervention Name(s)
Aquamantys
Other Intervention Name(s)
Aquamantys Malleable Bipolar Sealer with Light, 21 CFR 878.4400, Electrosurgery Bipolar Sealer
Intervention Description
Primary THA via the ASI approach will be performed using the Aquamantys Malleable Bipolar Sealer. The Aquamantys is a bipolar device that combines radio-frequency energy and saline to gently reach targeted tissue and provide a biomechanical seal. The saline acts as a conduit to allow the energy to penetrate the tissue from 1 to 2 mm where the collagen is transformed thus providing the seal. The saline also helps cool the tissue which allows for gentle handling of tissue, eliminating the black char that is a port for infection. The surgeon uses the Aquamantys to assist in tissue dissection, cauterize vessels, and to pre-treat fat pad in front of capsule prior to excision, to treat the entire anterior hip capsule prior to excision, treat oozing bone surfaces not covered by an implant.
Intervention Type
Device
Intervention Name(s)
standard electrocautery (Bovie)
Other Intervention Name(s)
electrocautery, Bovie
Intervention Description
Primary total hip arthroplasty via an anterior supine intermuscular approach will be performed with the assistance of standard electrocautery. The electrocautery is used in tissue dissection and to cauterize bleeding vessels.
Primary Outcome Measure Information:
Title
Perioperative Change in Hemoglobin Level
Description
All patients will undergo routine lab work perioperatively. No additional studies will be necessary for this protocol. Hemoglobin level will be first measured preoperatively at the time of preadmission testing, which must be performed not more than 30 days prior to surgery, and then measured on postoperative day one. The two levels will be compared to assess the decrease in hemoglobin level resulting from the surgical intervention.
Time Frame
From up to 30 days preoperative through postoperative day 1
Title
Perioperative Blood Transfusion Requirement
Description
Perioperative blood transfusion requirements will be recorded, including transfusions administered during the surgical intervention and throughout the acute hospital stay.
Time Frame
From the beginning of surgical intervention to hospital discharge, which averages 2 days and may be up to 1 week postoperative
Title
Perioperative Blood Loss
Description
Anesthesia and nursing records will be monitored for blood loss intraoperatively, and postoperatively via drain output. Drains will be pulled daily at 0600 and measured.
Time Frame
From beginning of surgical intervention through hospital discharge, which averages 2 days and may be up to 1 week
Secondary Outcome Measure Information:
Title
The development of complications in the wound, either as an inpatient or after discharge
Description
Wound care will be evaluated by a designee who will be blinded to the randomization. Wound will be evaluated for drainage, erythema, and ecchymosis. Additionally, the wound healing will be scored as: Healing better than expected, As expected, or Worse than expected. Wound evaluations will occur each postoperative day in hospital (average 2 days), at 6 weeks, and 1 year.
Time Frame
Wound evaluations will occur each postoperative day in hospital (average 2 days and up to 1 week), at 6 weeks, and 1 year.
Title
Length of stay
Description
Length of acute hospital stay will be recorded.
Time Frame
From admission through hospital discharge (average 2 days, up to 1 week)

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Undergoing primary unilateral total hip arthroplasty via the anterior supine intermuscular approach Patient is willing and able to complete all follow-up visits at 6 weeks and 1 year Exclusion Criteria: Patients with pre-existing known coagulopathy Patients on chronic Coumadin (Warfarin) therapy Patients receiving erythropoietin therapy for anemia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keith R Berend, MD
Organizational Affiliation
Joint Implant Surgeons, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Joint Implant Surgeons, Inc.
City
New Albany
State/Province
Ohio
ZIP/Postal Code
43054
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21411700
Citation
Barsoum WK, Klika AK, Murray TG, Higuera C, Lee HH, Krebs VE. Prospective randomized evaluation of the need for blood transfusion during primary total hip arthroplasty with use of a bipolar sealer. J Bone Joint Surg Am. 2011 Mar 16;93(6):513-8. doi: 10.2106/JBJS.J.00036.
Results Reference
result
PubMed Identifier
20097039
Citation
Zeh A, Messer J, Davis J, Vasarhelyi A, Wohlrab D. The Aquamantys system--an alternative to reduce blood loss in primary total hip arthroplasty? J Arthroplasty. 2010 Oct;25(7):1072-7. doi: 10.1016/j.arth.2009.10.008. Epub 2010 Jan 22.
Results Reference
result
PubMed Identifier
21964452
Citation
Mankin KP, Moore CA, Miller LE, Block JE. Hemostasis with a bipolar sealer during surgical correction of adolescent idiopathic scoliosis. J Spinal Disord Tech. 2012 Jul;25(5):259-63. doi: 10.1097/BSD.0b013e3182334ec5.
Results Reference
result
PubMed Identifier
21082586
Citation
Morris MJ, Berend KR, Lombardi AV Jr. Hemostasis in anterior supine intermuscular total hip arthroplasty: pilot study comparing standard electrocautery and a bipolar sealer. Surg Technol Int. 2010 Oct;20:352-6.
Results Reference
result
PubMed Identifier
18331175
Citation
Marulanda GA, Ulrich SD, Seyler TM, Delanois RE, Mont MA. Reductions in blood loss with a bipolar sealer in total hip arthroplasty. Expert Rev Med Devices. 2008 Mar;5(2):125-31. doi: 10.1586/17434440.5.2.125.
Results Reference
result
PubMed Identifier
16525984
Citation
Marulanda GA, Ragland PS, Seyler TM, Mont MA. Reductions in blood loss with use of a bipolar sealer for hemostasis in primary total knee arthroplasty. Surg Technol Int. 2005;14:281-6.
Results Reference
result
PubMed Identifier
20145794
Citation
Marulanda GA, Krebs VE, Bierbaum BE, Goldberg VM, Ries M, Ulrich SD, Seyler TM, Mont MA. Hemostasis using a bipolar sealer in primary unilateral total knee arthroplasty. Am J Orthop (Belle Mead NJ). 2009 Dec;38(12):E179-83.
Results Reference
result
Links:
URL
http://www.salientsurgical.com/
Description
Manufacturer's website; Related Info
URL
http://www.youtube.com/watch?v=s5O91NjEuCM
Description
Related info; animated sequence
URL
http://www.whichmedicaldevice.com/by-manufacturer/49/293/aquamantys-system
Description
Related info

Learn more about this trial

Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermuscular Approach Total Hip Arthroplasty

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