Brain Neuronal Networks, Chemosensory and Trigeminal Functions in Allo-HSCT

Sponsor
University of Oslo (Other)
Overall Status
Recruiting
CT.gov ID
NCT06003660
Collaborator
(none)
70
1
22.7
3.1

Study Details

Study Description

Brief Summary

The goal of this prospective, cohort study is to learn about smell, taste and trigeminal dysfunction in patients receiving allogeneic hematopoietic stem cell transplantation (allo-HSCT). The research team hypothesizes that treatment with allo-HSCT will induce:

  • Distortion of taste and smell and trigeminal functions like cooling, tingling, and burning sensations.

  • Reduced saliva production leading to oral dryness and dental caries.

  • Changes in the connectivity of the taste-, smell- and pain-cortical brain regions.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Participants will undergo various tests:
    • Smell function assessment with Sniffin' Sticks.

    • Taste function assessment with Taste Strips.

    • Oral trigeminal function assessment with von Frey filaments .

    • Salivary assessment with the Summated Xerostomia Inventory-Dutch questionnaire.

    • Salivary flow will be measured using salivary flow rate - stimulated whole saliva (SWS).

    • A clinical oral examination will be done to obtain a Clinical Oral Dryness Score.

    • Qualitative smell, taste and trigeminal dysfunction will be assessed using a questionnaire.

    • Radiological and clinical examinations will be performed to evaluate dental and oral mucosal status.

    • Quality of life using questionnaire.

    • Nutritional status using questionnaire.

    • Magnetic resonance imaging of the brain will be taken to capture regions-of-interest for the three different networks of interest; (i) the gustatory network reflecting changes in taste perception, (ii) the olfactory network, related to the changes in smell, and (iii) the pain matrix reflecting pain.

    There will be a comparisons between the patients and healthy controls.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    70 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    BrainFlavor: Brain Neuronal Networks and Chemosensory and Trigeminal Functions in Allogeneic Hematopoietic Stem Cell Transplantation - a Prospective Cohort-study
    Actual Study Start Date :
    Aug 10, 2023
    Anticipated Primary Completion Date :
    Dec 30, 2024
    Anticipated Study Completion Date :
    Jun 30, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    Patients

    Adult recipients of allo-HCST.

    Controls

    Healthy adult subjects

    Outcome Measures

    Primary Outcome Measures

    1. Olfactory (smell) function [1 year]

      Odour pens of the Sniffin' Sticks (Burghart Messtechnik, Wedel, Germany) will be used to test olfactory function (TDI). Scores will range from 0 - 48 where score ≤ 16.5 = anosmia (no sense of smell), score 16.6 - 30.5 = hyposmia (reduced sense of smell) and score >30.5 = normosmia (normal sense of smell)

    2. Self-reported olfactory (smell) function [1 year]

      Self-reported smell function will be assessed using a visual analogue scale (VAS) ranging from 0-10 where 0 indicates no smell function and 10 very good smell function.

    3. Gustatory (taste) function [1 year]

      Taste function will be evaluated by using taste strips ("Taste Strips "Burghart Messtechnik, Wedel, Germany) with four basic taste qualities (sweet, sour, salty and bitter) in 4 different concentrations each. Scores will range from 0 - 16 where 0 = ageusia (no sense of taste), 1 - 9 = hypogeusia (reduced sense of smell) and 10 - 16 = normogeusia (normal sense of taste)

    4. Self-reported gustatory (taste) function [1 year]

      Self-reported taste function will be assessed using a visual analogue scale (VAS) ranging from 0-10 where 0 indicates no taste function and 10 very good taste function.

    5. Oral pain assessment [1 year]

      Oral pain perception will be assessed by von Frey filaments. Scores will range from 0 -10 on a visual analogue scale (VAS) where 0 indicates no pain and 10 severe pain.

    6. Self-reported oral pain assessment [1 year]

      Self-reported oral pain will be assessed using a visual analogue scale (VAS) ranging from 0-10 where 0 indicates no oral pain and 10 severe oral pain.

    7. Functional brain connectivity [1 year]

      Functional connectivity analysis (fMRI) of three different networks of interest: (i) the olfactory network (ii) the gustatory, and (iii) the pain matrix. There are no specified quantitative units for these measurements.

    Secondary Outcome Measures

    1. Measured oral dryness [1 year]

      Saliva production will be measured using salivary flow rate - stimulated whole saliva (SWS). Hyposalivation is defined as a salivary secretion rate of ≤0.7 mL/min for SWS.

    2. Clinical oral dryness [1 year]

      Clinical oral dryness will be assessed using Clinical Oral Dryness Score (CODS). Scores will range from 0 to 10 points. Score 1-3 is considered mild oral dryness, 4-6 moderate and 7-10 severe oral dryness.

    3. Self-reported oral dryness [1 year]

      Self-reported oral dryness will be assessed using the Xerostomia Inventory (XI) questionnaire. Scores will range from 11 to 55 points, with values <14 considered as normal.

    4. Oral mucosal status [1 year]

      Oral mucosal status will be evaluated using mucosal-plaque index (MPS). Scores will range from 2 - 8 where 2 - 4 = good/acceptable, 5 - 6 = no acceptable and 7 - 8 = poor status

    5. Oral mucositis status [1 year]

      Oral mucosal status will be evaluated using the WHO mucositis grading ranging form 0 - 4 where 0 = no oral mucositis, 1 = erythema and soreness, 2 = ulcers, able to eat solids, 3 = ulcers, requires a liquid diet (due to mucositis), 4 = ulcers, alimentation not possible (due to mucositis)

    6. Nutritional status [1 year]

      Nutritional status will be evaluated using the Nutrition Risk Screening 2002 form. Scores range from 0-6. Patients with a score < 3 is considered to be of no nutritional risk. Patients with a score ≥ 3 is considered to be in nutritional risk.

    7. Quality of life evaluation [1 year]

      Quality of life will be assessed using the European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30). Scores range from 0-100. A high score indicates better quality of life and a low score indicates a worse quality of life.

    8. Oral health-related quality of life evaluation [1 year]

      Oral health-related quality of life will be assessed using the Oral Health Impact Profile-14 (OHIP-14) questionnaire. Scores range from 0-56. A high score indicates worse oral health-related quality of life, while a low score indicates better.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 50 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • patients receiving myeloablative conditioning for a first-time allo-HSCT and diagnosed with either a leukemia or a myelodysplastic syndrome

    Exclusion Criteria:
    • disorders affecting the oral cavity including poor tooth-status

    • those using drugs affecting the gustatory/olfactory functions

    • those with brain disorders

    • those who have a chronic disorder affecting the immune system, have cancer or who are pregnant.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Oslo Oslo Norway 0254

    Sponsors and Collaborators

    • University of Oslo

    Investigators

    • Study Director: Per Ole Iversen, phd, University of Oslo

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Per Ole Iversen, MD, Professor, University of Oslo
    ClinicalTrials.gov Identifier:
    NCT06003660
    Other Study ID Numbers:
    • 282886
    First Posted:
    Aug 22, 2023
    Last Update Posted:
    Aug 22, 2023
    Last Verified:
    Aug 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Aug 22, 2023