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Omental Transposition Surgery for Mild Alzheimer's Disease

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ClinicalTrials.gov Identifier: NCT02349191
Recruitment Status : Unknown
Verified March 2016 by Dr. Daniel Cottam, Bariatric Medicine Institute, Salt Lake City, UT.
Recruitment status was:  Not yet recruiting
First Posted : January 28, 2015
Last Update Posted : March 22, 2016
Sponsor:
Information provided by (Responsible Party):
Dr. Daniel Cottam, Bariatric Medicine Institute, Salt Lake City, UT

Tracking Information
First Submitted Date  ICMJE January 12, 2015
First Posted Date  ICMJE January 28, 2015
Last Update Posted Date March 22, 2016
Study Start Date  ICMJE March 2016
Estimated Primary Completion Date April 2017   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: January 23, 2015)
Incidence of surgical complications from beginning of anesthesia to discharge from Intensive Care Unit. [ Time Frame: Participants will be monitored for postoperative complications for the duration of their hospital stay, an expected average of 2 days. ]
surgical complications will be assessed from the anesthesia start time through hospital discharge.Total incidence (%) of complications will be calculated and reported,using Clavien-Dindo Classification of Surgical Complications.
Original Primary Outcome Measures  ICMJE Same as current
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: January 23, 2015)
  • Change in Alzheimer's Disease Assessment Scale - Cognition (ADAS-cog) score from baseline at 12 months. [ Time Frame: 12 months ]
    Percentage of score change, compared to baseline
  • Change in Montreal Cognitive Assessment (MoCA) score from baseline at 12 months [ Time Frame: 12 months ]
    Percentage of score change, compared to baseline
  • Change in General Practitioner Assessment of Cognition (GPCOG) score from baseline at 12 months [ Time Frame: 12 months ]
    Percentage of score change, compared to baseline
  • Change in Eight-item Informant Interview to Differentiate Aging and Dementia (AD8) score from baseline at 12 months [ Time Frame: 12 months ]
    Percentage of score change, compared to baseline
  • Change in Alzheimer's Disease Assessment Scale - Cognition (ADAS-cog) score from baseline at 24 months [ Time Frame: 24 months ]
    Percentage of score change, compared to baseline
  • Change in Montreal Cognitive Assessment (MoCA) score from baseline at 24 months [ Time Frame: 24 months ]
    Percentage of score change, compared to baseline
  • Change in General Practitioner Assessment of Cognition (GPCOG) score from baseline at 24 months [ Time Frame: 24 months ]
    Percentage of score change, compared to baseline
  • Change in Eight-item Informant Interview to Differentiate Aging and Dementia (AD8) score from baseline at 24 months [ Time Frame: 24 months ]
    Percentage of score change, compared to baseline
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Omental Transposition Surgery for Mild Alzheimer's Disease
Official Title  ICMJE A Prospective, Single Site, Single Arm, Non-randomized, Interventional Study to Evaluate the Safety and Effectiveness of Omental Transposition Surgery for Patients With Alzheimer's Disease.
Brief Summary

This study is a prospective, single arm, non-randomized, interventional study to evaluate the safety and effectiveness of Omental transposition (OT) in subjects with early stage AD.

Within-subjects (repeated-measures) design will be utilized to compare follow-up outcomes to baseline.

The following assessments will be performed at baseline, then at 1, 3, 6, 12, and 24 months following surgery:

  • Montreal Cognitive Assessment (MoCA)
  • Alzheimer's Disease Assessment Scale-Cognition (ADAS-Cog)
  • General Practitioner Assessment of Cognition (GPCOG)
  • Eight-item Informant Interview to Differentiate Aging and Dementia (AD8) Subjects who have early stage AD confirmed by a neuropsychological test (MoCA) and who are healthy enough to undergo surgery.

The experimental procedure to be performed is omental transposition (OT) surgery. It will be performed as a laparoscopic or open procedure for omental lengthening and an open procedure for brain access, with a general surgeon performing the omental lengthening/tunneling and a neurosurgeon performing brain access/brain biopsy/omental placement on brain.

Up to twenty-five (25) subjects, with the first 5 subjects being part of a learning curve group and the next 20 subjects being part of the experimental group.

The duration of each subject's participation will be approximately 25 months from screening through the 24 month follow-up visit.

Detailed Description

The experimental procedure to be performed is omental transposition surgery, during which a general surgeon and a neurosurgeon work as a team to transpose a pedicle omental graft to the surface of the brain. The general surgeon is responsible for performing a laparotomy/laparoscopy, elongating the omentum into a long pedicle and developing an extensive subcutaneous tunnel up the chest and neck to the head. The neurosurgeon is responsible for performing the craniotomy and securing the omentum on the brain.

Creating an intact omental pedicled flap requires the services of a general surgeon and neurosurgeon. The first step in the operation is to obtain access to the abdominal cavity laparoscopically using four 5cm trocars, or via laparotomy through an upper midline incision. The omentum is then removed from the transverse colon, after which it is separated from its proximal and central attachments to the stomach. The omentum detachments are made directly on the greater curvature of the stomach, leaving the gastroepiploic arteries and veins within the still-connected omentum apron.

Final separation of the omentum from the proximal portion of the stomach is done by dividing the left gastroepiploic vessels, which at the highest proximal level on the stomach become the short gastric vessels. The vascular connections to and from the omentum are now maintained solely from the right gastric and right gastroepiploic vessels. In order for the omental pedicle graft to reach the brain without tension, further surgical tailoring of the omentum is carried out, with care being taken to ensure the preservation of a major omental artery and vein.

After the omentum has been lengthened to an appropriate extent to reach the head, several small (3- to 4-inch) transverse incisions are made on the chest wall slightly lateral to the midline, with the side of the midline to make the transverse incisions depending on which cerebral hemisphere the omentum is to be placed. These transverse incisions are connected subcutaneously, thus creating a tunnel that begins at the upper pole of the midline abdominal incision and travels subcutaneously, up the chest wall and neck to behind the ear.

Although the subcutaneous tissue behind the ear is extremely dense, it is essential that the tunnel at this location be at least 2-3 finger lengths in width so that there is no constriction on the omentum in this particular area within the tunnel. As the omentum in the tunnel passes behind the ear, it goes beneath the base of the scalp flap that had been previously dissected in making the initial craniotomy incision.

The neurosurgery portion of the operation involves removal of a single piece of bone over the temporal-frontal area, opening the dura mater, followed by the removal of patches of arachnoid membrane, with care being taken to avoid blood vessels on the surface of the brain.

At this point in the operation, the omentum is laid directly upon the parietal-temporal-frontal area, after which the dura mater is sutured to the omentum. It is not necessary that the edges of the omentum be applied to the cut edges of the dura since the omentum can be tucked under the edges of the dura for greater coverage of the brain. The edges of the dura are then sewn to the top surface of the omentum using absorbable sutures and the craniotomy is closed.

Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Alzheimer's Disease
Intervention  ICMJE Procedure: Omental transposition for mild Alzheimers disease
An omental pedicle is brought from the abdomen underneath the skin and sewn to the dura matter of the brain via a craniotomy.
Study Arms  ICMJE Experimental: Interventional cohort
Omental transposition for mild Alzheimers Disease
Intervention: Procedure: Omental transposition for mild Alzheimers disease
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Unknown status
Estimated Enrollment  ICMJE
 (submitted: January 23, 2015)
25
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE May 2019
Estimated Primary Completion Date April 2017   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  1. Male or female subjects between 60 to 85 years of age
  2. Montreal Cognitive Assessment (MoCA) score of 11 to 18 (mild AD)
  3. Healthy enough to undergo the surgical procedure based on surgical risk factor definitions (ASA ≤ 3, using the ASA classification)
  4. Must be able to read and understand English in order to complete all AD assessments
  5. All medical illnesses other than dementia must be well controlled
  6. Must have legally authorized caregiver if incapable of making their own decisions who is willing and able to perform the following:

    1. provide informed consent if the subject is unable to do so;
    2. monitor the subject;
    3. answer informant based questionnaires;
    4. provide transportation and accompany the subject to all visits
  7. Subject or caregiver is willing and able to provide written informed consent and assent (if applicable)
  8. Subject and/or caregiver are willing to comply with the study procedures and complete the entire study as specified in the protocol

Exclusion Criteria:

  1. Life expectancy < 2 years
  2. Subject who had or has cancer and is undergoing cancer therapy
  3. Previous course of abdominal, cranial or neck radiotherapy or chemotherapy
  4. Patients with neck calcifications may be excluded
  5. Subject with uncontrolled heart disease, renal disease, or liver disease
  6. Subject with diabetes mellitus whose glycoslated Hb (A1C) > 7
  7. Complete blood count (CBC) with white blood cell <4,000 or platelets >125,000
  8. Subject with uncontrollable hypertension (HTN)
  9. Subject with previous abdominal surgery or disorder that could negatively influence the outcome of the OT surgery
  10. Subject who has had a craniotomy in the past
  11. Recent major surgery within the past 6 months
  12. Use of cholinesterase inhibitors within the last 30 days and inability to not take cholinesterase inhibitors throughout the length of the study (about 25 mos)
  13. Subject uses non-prescribed drugs of abuse or has a history of drug or alcohol abuse/dependence
  14. Use of anticoagulants other then anti-platelet medications
  15. Subject has significant central nervous system (CNS) disorder other than Alzheimer's disease
  16. Subject has clinical evidence or history of stroke, transient ischemic attack, significant head injury or other unexplained or recurrent loss of consciousness ≥15 minutes
  17. Major depressive disorder, schizophrenia, other psychotic disorders, or bipolar disorder
  18. Subject has epilepsy
  19. Patients with severe extra pyramidal signs
  20. Patients with plastic surgery of the neck or face
  21. Subject resides in hospital or moderate to high dependency continuous care facility
  22. Non-English speaking subjects and/or caregivers
  23. Subject has any condition that, in the opinion of the Investigator would preclude the use of the study procedure, may interfere with the evaluation of the procedure-related outcomes, or preclude the subject from completing the follow-up requirements
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 65 Years to 85 Years   (Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Not Provided
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT02349191
Other Study ID Numbers  ICMJE Cottam - 1
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party Dr. Daniel Cottam, Bariatric Medicine Institute, Salt Lake City, UT
Study Sponsor  ICMJE Bariatric Medicine Institute, Salt Lake City, UT
Collaborators  ICMJE Not Provided
Investigators  ICMJE Not Provided
PRS Account Bariatric Medicine Institute, Salt Lake City, UT
Verification Date March 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP