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A Personalised Radiosurgery Procedure for People With Trigeminal Neuralgia to Improve Pain, Quality of Life and Reduce Complications

Primary Purpose

Trigeminal Neuralgia, Multiple Sclerosis, Pain

Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Gamma Knife Radiosurgery (GKRS) personalised procedure
GKRS standard care
Sponsored by
University of Leeds
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Trigeminal Neuralgia focused on measuring multiple sclerosis, trigeminal neuralgia, Pain, Quality of life

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Subject has idiopathic TN or MS-related TN.
  2. Subject is available for follow up.

4. Subject can understand the informed consent form in English. 5. Age over 18 years at the time of signing the Informed Consent Form 6. Have been treatment planned to receive GKRS treatment

Exclusion Criteria:

Patients who:

  1. Have no capacity to complete written informed consent
  2. Do not understand English
  3. Repeat GKRS treatment

Sites / Locations

  • Sheffield royal hallamshire hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control arm

Intervention

Arm Description

Standard care

Outcomes

Primary Outcome Measures

Barrow Neurological Institute (BNI) pain measure
BNI Pain Scale (BNI-PS), 5-level categories (scale range: 1-5)
Barrow Neurological Institute (BNI) numbness measure
BNI Numbness Scale (BNI-NS), 5-level categories (scale range: 1-5)

Secondary Outcome Measures

Current medication and dosage
Vision complications
Recorded as adverse events such as blurred vision, double vision, or water eyes
Motor impairment
Assessed through a battery of test with a performance score (range: 1-100)
Cognitive impairment
Assessed through a battery of test with a performance score (range: 1-100)

Full Information

First Posted
September 18, 2019
Last Updated
June 26, 2023
Sponsor
University of Leeds
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1. Study Identification

Unique Protocol Identification Number
NCT04117035
Brief Title
A Personalised Radiosurgery Procedure for People With Trigeminal Neuralgia to Improve Pain, Quality of Life and Reduce Complications
Official Title
A Personalised Radiosurgery Procedure for People With Trigeminal Neuralgia to Improve Pain, Quality of Life and Reduce Complications - a Confidence in Concept Pilot Study (PROMOTION)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Leeds

4. Oversight

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

5. Study Description

Brief Summary
The aim of this study is to evaluate prospectively the feasibility and impact of personalised gamma knife radiosurgery treatment protocol versus current standard protocol for people with idiopathic or Multiple Sclerosis-related Trigeminal Neurolgia (MS related TN) on effectiveness in pain relief, the development of morbidity and quality of life. Patients with TN or MS-related TN are referred to the National Centre for Stereotactic Radiosurgery in Sheffield for clinical consultation, and will undergo gamma knife radiosurgery (GNRS) for treating trigeminal neuralgia if eligible. The GKRS treatment is provided as a standard National Health Service (NHS) routine care. The current procedure has been proven to be safe and effectiveness in reducing the pain caused by TN. The current GKRS treatment protocol performs the treatment on the trigeminal nerve close to the brainstem, which might result in higher complication rate (mainly facial numbness). This study will conduct a pilot randomised controlled trial to evaluate an alternative treatment protocol, which will perform the GKRS treatment at the retrogasserian zone (further away from the brainstem). This treatment protocol has been widely used in Europe and USA, and is safe and effective. Most studies adopting this protocol have shown less complication rate after treatment.
Detailed Description
Trigeminal neuralgia (TN) is a condition of excruciating facial pain characterized by brief, repeated, electric shock-like pains. Like idiopathic TN, people with multiple sclerosis (MS) related TN (PwMSTN) often suffer from episodic facial pain (often excruciating) that may be related to demyelination of the trigeminal pathways. It is estimated that people with multiple sclerosis (PwMS) are 20 times more likely to present with TN symptoms than non-MS people and a recent review estimated that 4-8% of PwMS have TN. Patients with TN or MS-related TN who no longer respond to treatment often opt for non-invasive gamma knife radiosurgery (GKRS), with variable outcomes. Factors, such as patient characteristics, target treatment location and radiation dosage, could affect the efficacy of pain relief and result in post-surgical morbidity. There is no consensus of the best GKRS target treatment location or the optimal radiation dosage for GKRS treatment among centers, this results in great variability across centers in patient outcomes of pain control and morbidity. This prospective surgical pilot study will recruit PwTN and PwMS-related TN from the National Center for Stereotactic Radiosurgery, Sheffield, to evaluate the impact of a personalized GKRS treatment protocol on safety, efficacy (pain control) and morbidity. The personalized procedure will target the treatment location on trigeminal nerve further away from the brain stem as compared to the current standard treatment location that is closer to the brain stem. The personalized procedure may reduce the radiation dose to the brain stem and then reduce the adverse effects of the treatment. The recruited PwTN and PwMS-related TN will be randomly allocated to either the personalized GKRS treatment protocol group or the standard GKRS treatment protocol group. The efficacy in pain relief and morbidity will be evaluated between the treatment groups at 6 months and 12 months post-surgery. This study does not have main ethical, legal issues. The GKRS treatment is provided as routine NHS care, and the study will only alter the treatment location for those patients who would normally go through the standardtreatment protocol. Therefor there will be no management issues. Information collected during this study will be kept confidential. All data collected for this study will be kept safely and securely on secure NHS computer server and paper records at the clinic. All data will be handled strictly according to the University of Leeds privacy notice for research participants

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trigeminal Neuralgia, Multiple Sclerosis, Pain
Keywords
multiple sclerosis, trigeminal neuralgia, Pain, Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
single-blinded randomised control pilot study
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control arm
Arm Type
Placebo Comparator
Arm Description
Standard care
Arm Title
Intervention
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Gamma Knife Radiosurgery (GKRS) personalised procedure
Intervention Description
Personalised GKRS treatment
Intervention Type
Procedure
Intervention Name(s)
GKRS standard care
Intervention Description
Standard GKRS treatment
Primary Outcome Measure Information:
Title
Barrow Neurological Institute (BNI) pain measure
Description
BNI Pain Scale (BNI-PS), 5-level categories (scale range: 1-5)
Time Frame
6 MONTHS
Title
Barrow Neurological Institute (BNI) numbness measure
Description
BNI Numbness Scale (BNI-NS), 5-level categories (scale range: 1-5)
Time Frame
6 MONTHS
Secondary Outcome Measure Information:
Title
Current medication and dosage
Time Frame
12 MONTHS
Title
Vision complications
Description
Recorded as adverse events such as blurred vision, double vision, or water eyes
Time Frame
12 MONTHS
Title
Motor impairment
Description
Assessed through a battery of test with a performance score (range: 1-100)
Time Frame
12 MONTHS
Title
Cognitive impairment
Description
Assessed through a battery of test with a performance score (range: 1-100)
Time Frame
12 MONTHS

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject has idiopathic TN or MS-related TN. Subject is available for follow up. 4. Subject can understand the informed consent form in English. 5. Age over 18 years at the time of signing the Informed Consent Form 6. Have been treatment planned to receive GKRS treatment Exclusion Criteria: Patients who: Have no capacity to complete written informed consent Do not understand English Repeat GKRS treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jianhua Wu, PhD
Phone
0113 343 3431
Email
j.h.wu@leeds.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Sakina Edwebi, PhD
Phone
07825814912
Email
S.Edwebi@leeds.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jianhua Wu, PhD
Organizational Affiliation
University of Leeds
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheffield royal hallamshire hospital
City
Sheffield
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alison Loescher, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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A Personalised Radiosurgery Procedure for People With Trigeminal Neuralgia to Improve Pain, Quality of Life and Reduce Complications

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