search
Back to results

Exploring the Impact of Perioperative Galacto-Oligosaccharides (GOS) on Stress, Anxiety and Cognition

Primary Purpose

Anxiety, Pain, Surgery

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Galacto-Oligosaccharide
Maltodextrin (Placebo)
Sponsored by
Jeff Taekman, M.D.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Anxiety focused on measuring perioperative, surgery, pain, anxiety, post operative cognitive dysfunction, cognition

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients undergoing anterior cervical discectomy and fusion

Exclusion Criteria:

  • Pregnancy
  • Breast Feeding Women
  • Diagnosis of Depression
  • Diagnosis of mental or behavioral disorder
  • Recent anxiolytic use (within 1 week of enrollment)
  • Long-term opiate use (greater than 1 week prior to enrollment)
  • Recent systemic steroid use (within 1 week of enrollment)
  • Diagnosis of cancer
  • Oral or intravenous antibiotic use within 1 month of enrollment

Sites / Locations

  • Duke University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Galacto-Oligosaccharides (GOS)

Maltodextrin (Placebo)

Arm Description

Clasado Biosciences Limited will provide Bimuno Pastilles for the clinical trial. Each pastille contains 0.92g GOS and will be taken 3 times per day. Following informed consent, subjects will be issued prepackaged GOS pastilles to be taken three times daily up until the evening prior to surgery. Subjects will be randomly assigned to receive GOS prebiotics. Each subject has an equal chance of receiving GOS or placebo. GOSn will be administered in the hospital when patient reinstitutes oral intake. GOS will be issued to each subject to last until the day of their scheduled follow-up for POCD (approximately 1.5 months post surgery).

Clasado Biosciences Limited will provide placebo (Maltodextrin) for the clinical trial. Each pastille contains maltodextrin and will be taken 3 times per day. Following informed consent, subjects will be issued prepackaged pastilles to be taken three times daily up until the evening prior to surgery. Subjects will be randomly assigned to receive GOS prebiotics or placebo. Each subject has an equal chance of receiving GOS or placebo. Placebo will be administered in the hospital when patient reinstitutes oral intake. Placebo will be issued to each subject to last until the day of their scheduled follow-up for POCD (approximately 1.5 months post surgery).

Outcomes

Primary Outcome Measures

Change in Waking Salivary Cortisol

Secondary Outcome Measures

Changes in pain perception
Collected through Visual Analog Scale.
Changes in cognition
Hopkins Verbal Learning Test - Revised (HVLT-R)
Changes in perceived stress
Subjects will complete web-based versions of the State-Trait Anxiety Scale.
Changes in perceived stress
Subjects will complete web-based versions Hospital Anxiety and Depression Scale-HADS.
Changes in perceived stress
Subjects will complete web-based versions Visual Analog Anxiety Scale.
Changes in cognition
Randt Short Story Memory Test
Changes in cognition
Modified Visual Reproduction Test from the Wechsler Memory Scale
Changes in cognition
Weschsler Adult Intelligence Scale - Revised (WAIS-R)
Changes in cognition
Trail Making Test
Changes in cognition
Grooved Pegboard
Changes in cognition
Mini Mental Status Exam (MMSE)
Suicidal ideation and behavior
Columbia-Suicide Severity Rating Scale (C-SSRS)

Full Information

First Posted
October 24, 2016
Last Updated
January 30, 2018
Sponsor
Jeff Taekman, M.D.
search

1. Study Identification

Unique Protocol Identification Number
NCT02953691
Brief Title
Exploring the Impact of Perioperative Galacto-Oligosaccharides (GOS) on Stress, Anxiety and Cognition
Official Title
Exploring the Impact of Perioperative Galacto-Oligosaccharides (GOS) on Stress, Anxiety and Cognition
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Withdrawn
Why Stopped
Lack of Study Substance
Study Start Date
June 9, 2017 (Actual)
Primary Completion Date
January 1, 2018 (Actual)
Study Completion Date
January 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jeff Taekman, M.D.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall objective of this proposal is to explore the association between the administration of the prebiotics GOS (trade name: Bimuno Travelaid; generic name:B galacto-oligosaccharides) with pain, anxiety, and cognitive function in the perioperative period. The investigators' central hypothesis is subjects who consume GOS in the perioperative period will demonstrate lower levels of salivary cortisol before, during, and after their operative procedures. In addition, the investigators expect subjects who consume GOS to have lower perceived levels of anxiety during the perioperative period. Finally, the investigators hypothesize that subjects who consume perioperative GOS will perform better on tests of cognition in the postoperative period. Such a finding would be beneficial in that administration of GOS in the perioperative period offers a safe and inexpensive adjunct to current medical management of perioperative anxiety.
Detailed Description
AIM 1: In anterior cervical decompression and fusion (ACDF) subjects, explore the association between prebiotics, anxiety, and pain. Studies have recently elucidated a link between certain prebiotics and lower perceived anxiety as well as biomarkers of stress. In this aim the investigators will explore the association between consumption of prebiotics and their relationship to perioperative anxiety / physiological stress response. The investigators hypothesize that subjects who receive prebiotics will have lower perioperative anxiety and stress versus control as measured by standardized surveys and biomarkers. Furthermore, the investigators hypothesize that lower anxiety will result in lower postoperative pain scores. AIM 2: In ACDF patients, explore the association between GOS and post-operative cognitive dysfunction. Stress and anxiety is known to impair cognitive function. In addition, in preclinical studies, the administration of distinct keystone bacterial strains improves cognitive function in an anxious mouse model. In humans, prebiotics and probiotics have been shown to ameliorate the stress response. In this aim the investigators seek to explore the association between prebiotics and perioperative cognitive outcomes in humans. The investigators will perform cognitive function testing using the same time-tested battery used in the department to study post-operative cognitive decline (POCD). Subjects will be tested for cognitive function preoperatively (T1) and at 1.5 months post-op (T4). The investigators hypothesize that patients receiving prebiotics during the perioperative period will show less post-operative cognitive dysfunction than controls. A total of 8 subjects will be recruited from the Neurosurgery Clinics of Duke University Health System. The target population will include subjects undergoing ACDF. Exclusion criteria will include: pregnant women, age<21 years, a diagnosis of depression, mental or behavioral disorder, recent anxiolytic use, long-term opiate use, oral contraceptive use, or recent antibiotic use.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Pain, Surgery
Keywords
perioperative, surgery, pain, anxiety, post operative cognitive dysfunction, cognition

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Galacto-Oligosaccharides (GOS)
Arm Type
Experimental
Arm Description
Clasado Biosciences Limited will provide Bimuno Pastilles for the clinical trial. Each pastille contains 0.92g GOS and will be taken 3 times per day. Following informed consent, subjects will be issued prepackaged GOS pastilles to be taken three times daily up until the evening prior to surgery. Subjects will be randomly assigned to receive GOS prebiotics. Each subject has an equal chance of receiving GOS or placebo. GOSn will be administered in the hospital when patient reinstitutes oral intake. GOS will be issued to each subject to last until the day of their scheduled follow-up for POCD (approximately 1.5 months post surgery).
Arm Title
Maltodextrin (Placebo)
Arm Type
Placebo Comparator
Arm Description
Clasado Biosciences Limited will provide placebo (Maltodextrin) for the clinical trial. Each pastille contains maltodextrin and will be taken 3 times per day. Following informed consent, subjects will be issued prepackaged pastilles to be taken three times daily up until the evening prior to surgery. Subjects will be randomly assigned to receive GOS prebiotics or placebo. Each subject has an equal chance of receiving GOS or placebo. Placebo will be administered in the hospital when patient reinstitutes oral intake. Placebo will be issued to each subject to last until the day of their scheduled follow-up for POCD (approximately 1.5 months post surgery).
Intervention Type
Drug
Intervention Name(s)
Galacto-Oligosaccharide
Intervention Description
Mixture produced from lactose utilizing the transgalactosidic activity of Bifidobacterium bifidum NCIMB 41171 beta-galactosidase
Intervention Type
Drug
Intervention Name(s)
Maltodextrin (Placebo)
Intervention Description
Maltodextrin is a polysaccharide commonly used as a food additive. It is produced from starch by partial hydrolysis.
Primary Outcome Measure Information:
Title
Change in Waking Salivary Cortisol
Time Frame
Morning after Preop Clinic Visit (2 weeks prior to surgery), 2-hours before surgery, 1-day after surgery, 6-week follow-up visit
Secondary Outcome Measure Information:
Title
Changes in pain perception
Description
Collected through Visual Analog Scale.
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 2-hours before surgery, 30 minutes after surgery, 1-day after surgery, 6 week follow-up visit
Title
Changes in cognition
Description
Hopkins Verbal Learning Test - Revised (HVLT-R)
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 6 week follow-up visit
Title
Changes in perceived stress
Description
Subjects will complete web-based versions of the State-Trait Anxiety Scale.
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 2-hours before surgery, 1-day after surgery, 6 week follow-up visit
Title
Changes in perceived stress
Description
Subjects will complete web-based versions Hospital Anxiety and Depression Scale-HADS.
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 2-hours before surgery, 1-day after surgery, 6 week follow-up visit
Title
Changes in perceived stress
Description
Subjects will complete web-based versions Visual Analog Anxiety Scale.
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 2-hours before surgery, 30 minutes after surgery, 1-day after surgery, 6 week follow-up visit
Title
Changes in cognition
Description
Randt Short Story Memory Test
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 6 week follow-up visit
Title
Changes in cognition
Description
Modified Visual Reproduction Test from the Wechsler Memory Scale
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 6 week follow-up visit
Title
Changes in cognition
Description
Weschsler Adult Intelligence Scale - Revised (WAIS-R)
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 6 week follow-up visit
Title
Changes in cognition
Description
Trail Making Test
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 6 week follow-up visit
Title
Changes in cognition
Description
Grooved Pegboard
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 6 week follow-up visit
Title
Changes in cognition
Description
Mini Mental Status Exam (MMSE)
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 6 week follow-up visit
Title
Suicidal ideation and behavior
Description
Columbia-Suicide Severity Rating Scale (C-SSRS)
Time Frame
Preop Clinic Visit (2 weeks prior to surgery), 2-hours before surgery, 1-day after surgery, 6 week follow-up visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients undergoing anterior cervical discectomy and fusion Exclusion Criteria: Pregnancy Breast Feeding Women Diagnosis of Depression Diagnosis of mental or behavioral disorder Recent anxiolytic use (within 1 week of enrollment) Long-term opiate use (greater than 1 week prior to enrollment) Recent systemic steroid use (within 1 week of enrollment) Diagnosis of cancer Oral or intravenous antibiotic use within 1 month of enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey M Taekman, M.D.
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25449699
Citation
Schmidt K, Cowen PJ, Harmer CJ, Tzortzis G, Errington S, Burnet PW. Prebiotic intake reduces the waking cortisol response and alters emotional bias in healthy volunteers. Psychopharmacology (Berl). 2015 May;232(10):1793-801. doi: 10.1007/s00213-014-3810-0. Epub 2014 Dec 3.
Results Reference
background
PubMed Identifier
24838095
Citation
Tillisch K. The effects of gut microbiota on CNS function in humans. Gut Microbes. 2014 May-Jun;5(3):404-10. doi: 10.4161/gmic.29232. Epub 2014 May 16.
Results Reference
background

Learn more about this trial

Exploring the Impact of Perioperative Galacto-Oligosaccharides (GOS) on Stress, Anxiety and Cognition

We'll reach out to this number within 24 hrs