Intraoperative Neurophysiological MonitoringIONMNCT04443465
Patient Experiences of IONM and Outcomes
An observational study of Intraoperative Neurophysiological Monitoring and Complication, run by King's College Hospital NHS Trust at 1 site in United Kingdom.
Trial summary
Resection of brain tumours forms a large proportion of work in brain surgery. One important aspect is to minimize damage to normal brain structures during this process. This improves patient outcomes and reduces complications. Read more about this study
- Who is it for?
- Ages 10 years and older
- Conditions the study is for
- Intraoperative Neurophysiological Monitoring, Complication, Intraoperative Complications
- How many people
- 50 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 10 Oct 2018to 10 Mar 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 10 years and older
- All sexes
- Child, Adult, Older adult
Study population: Adults and children aged 10 and above undergoing brain or spinal surgery with intra operative neurophysiological monitoring with intravenous anaesthesia
Who may be able to join
- All patients aged 10 and above undergoing elective neurosurgery guided by IONM will be recruited with informed consent.
Who cannot join
- Lack of informed consent and who are unable to communicate verbally.-
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Physical Effects and Emotional Experiences of Intra-operative Neuro-monitoring (IONM)
Resection of brain tumours forms a large proportion of work in brain surgery. One important aspect is to minimize damage to normal brain structures during this process. This improves patient outcomes and reduces complications. To identify normal brain structures from the abnormal tumours, the brain surgeons use a 'guidance' technique called intraoperative neuro-monitoring (IONM).
IONM uses various electrodes to observe spontaneous electrical activity of the brain or its reaction to a stimulus such as muscle contraction, light or sound. It is now becoming common practice for neurosurgeons to use this tool during brain and spinal surgery to provide a real-time feedback under anaesthesia to help them minimise injury to important and normal brain and spine structures.
Read more
IONM interpretation needs fulfilment of multiple preconditions and major modifications to the anaesthetic to reduce its inaccuracies. This invites added risks and complications such as awareness, convulsions and heart problems under anaesthesia. A team approach between the surgeon, anaesthetist and neurophysiologist (IONM specialist) is also crucial to obtain meaningful results. Therefore, the usefulness of this technique is still not perfect.
Although, benefits of IONM are obvious, information on associated complications and patient experience are not commonly found in the literature. Information on other effects such as hormonal balance and tumour recurrence are also scarce. In general, these aspects have little scientific exploration.
There are anecdotal reports of recurrent seizures during IONM leading to serious heart problems, teeth and tongue damage due to grinding and postoperative calf muscle injury necessitating further surgery to save limbs. Neither of these is in the literature including unorthodox treatments such as the use of cold saline to control IONM triggered fits.
This study is designed to observe complications and outcome and explore patient experiences following IONM in an observational capacity not interfering with the clinical management or treatment of these patients. The investigators intend to interview the participants after surgery, at a convenient time before leaving hospital to understand their views and experiences during and after surgery and their general progress in the following one year.
Read the detailed description
INTRODUCTION Intraoperative neuro-monitoring (IONM) is a 'SAT NAV' used by neurosurgeons to prevent injury to normal structures during brain and spinal surgery under anaesthesia. It involves the use of surface and implanted electrodes to observe spontaneous electrical activity of the brain or evoked responses to an electrical stimulus (motor, visual or auditory). This requires major modifications to the anaesthetic that provides lighter planes of anaesthesia with no muscle relaxation inviting added risks and complications such as awareness, seizures and cardiac events.
This cohort study over a period of one year will include a qualitative enquiry of patient experience and a quantitative evaluation of the immediate postoperative course and complications at 28 days and 1 year. It will explore the relatively unknown area of emotional experiences of participants under anaesthesia who undergo various types of neuro stimulation and related post-operative sequelae. The results are expected to assist improve patient experiences and outcomes.
BACKGROUND AND RATIONALE Resections of brain tumours constitute a significant proportion of work in neurosurgery. One important aspect is minimizing injury to normal neural structures during this process to improve outcomes of such operations and reduce complications. This involves intraoperative neuro-monitoring (IONM).
IONM uses surface and implanted electrodes to observe spontaneous electrical activity of the brain or evoked response to a motor, visual or auditory stimulus. It is now becoming common practice for neurosurgeons to use this tool during brain and spinal surgery to provide a real-time feedback under anaesthesia to help them minimise injury to critical and normal neural structures by 'mapping' normal from abnormal areas of the brain.
IONM interpretation needs fulfilment of multiple preconditions and major modifications to the anaesthetic to reduce its inaccuracies. This invites added risks and complications such as awareness, seizures and cardiac events. A team approach is also crucial to obtain meaningful results. Therefore, the utility of this technique is still evolving based on personal experiences and perceptions and the understanding between the surgeons, anaesthetists and neurophysiologists.
Although, benefits of IONM are obvious, data on associated post-operative morbidity and patient experience and complications are scarce. The data is also scarce on tumour recurrence or tumour behaviour following IONM guided neurosurgery. More precise excision may reduce tumour recurrence. On the other hand IONM related electrical stimulation may impose humoral effects on tumour behaviour. These aspects have little scientific exploration.
There are anecdotal reports of recurrent seizures during IONM leading to cardiac events such as asystole, teeth grinding and damage and tongue injury in the absence of a 'bite block' and postoperative calf muscle necrosis necessitating fasciotomies. Neither of these is in the literature including the unorthodox effective treatments used such as pouring 'cold' saline on the surface of the brain to control seizures.
The study will take place in a major neurosurgical centre in the UK that uses IONM. Therefore, the study population is vast for appropriate sampling and recruitment.
STUDY DESIGN This is an observational cohort study based on data retrieved from clinical notes and direct patient interview in hospital. The qualitative enquiry will address emotional aspects and the process experience. The quantitative survey will investigate morbidity (post-operative recovery, complications) and outcomes including mortality at 28 days and 1-year follow-up.
The eligible patients will be identified by the published elective neurosurgery lists and approached for informed consent before surgery at the time of preoperative assessment.
The anaesthetist or the surgeon directly involved with his/her clinical care will first approach the patient and subsequently introduced to the medical student for post-operative data collection. Their demographic data, disease data, and neurological assessment scores will be obtained from medical records. Direct patient interviews will be carried out by the investigators postoperatively, using a structured open questionnaire format. This activity will merge with the postoperative clinical rounds where possible.
All patients undergoing elective neurosurgery guided by IONM will be eligible for the study and recruited with informed consent. The exclusion criteria shall be aged less than 10 years, lack of informed consent and who are unable to communicate verbally.
A convenient sample of 50 is a realistic number of patients who can be recruited within a 3-month period at this centre. However, the qualitative enquiry may be stopped at an earlier time if the data collected is felt to be at the saturation point by the investigators. The participants shall be followed up at 28 days and 1-year post surgery.
Continuous data will be described and analysed based on their distribution, be it parametric or non-parametric. Dichotomous data will be described as number of patients/episodes and percentage.The patient experiences reported will be subjected to a thematic analysis following the principles of qualitative research grounded theory.
- Conditions
- Intraoperative Neurophysiological Monitoring, Complication, Intraoperative Complications, Postoperative Complications
- Medical subject headings
- Intraoperative Complications, Postoperative Complications
What is being measured
The primary outcome is the main question the study is designed to answer.
Experiences of participants who undergo intra-operative neurophysiological monitoring under anaesthesia
A qualitative study of patient experiences by thematic analysis
Measured: 2 years
Secondary outcomes (3)
IONM related postoperative sequel during post surgical recovery in hospital
Perioperative adverse events description
Measured: 2 years
Mortality at 28 day and 1 year follow up
Mortality rates at 28 days and 1 year
Measured: 2 years
Morbidity at 28 days and 1 year follow up
Residual weaknesses and disability
Measured: 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jun 2020
- Study start10 Oct 2018
- Primary completion10 Mar 2020
- Study completion10 Mar 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (7)Papers the sponsor has linked to this study.
- Other trials for Intraoperative Neurophysiological MonitoringStudies of the same condition, open and under way.
- More trials run by King's College Hospital NHS TrustThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- King's College Hospital NHS Trust
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Chulananda Goonasekera, PhD, Principal investigator, Kings College Hospital NHS Trust, London
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04443465
- Sponsor's protocol ID
- IRAS 239002
- Acronym
- IONM
- Status last verified
- Mar 2020
- First submitted
- 10 Oct 2018
- Last updated
- 23 Jun 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: Anonymised qualitative and quantitative data
Publications
Stecker MM. A review of intraoperative monitoring for spinal surgery. Surg Neurol Int. 2012;3(Suppl 3):S174-87. doi: 10.4103/2152-7806.98579. Epub 2012 Jul 17.
PubMed 22905324Jameson LC, Sloan TB. Monitoring of the brain and spinal cord. Anesthesiol Clin. 2006 Dec;24(4):777-91. doi: 10.1016/j.atc.2006.08.002.
PubMed 17342964Arnold PM. Use of intraoperative monitoring in children. J Neurosurg Pediatr. 2014 Jun;13(6):589. doi: 10.3171/2013.9.PEDS13439. Epub 2014 Apr 4. No abstract available.
PubMed 24702618Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet. 1986 Feb 8;1(8476):307-10.
PubMed 2868172Jameson LC, Janik DJ, Sloan TB. Electrophysiologic monitoring in neurosurgery. Anesthesiol Clin. 2007 Sep;25(3):605-30, x. doi: 10.1016/j.anclin.2007.05.004.
PubMed 17884710Soghomonyan S, Moran KR, Sandhu GS, Bergese SD. Anesthesia and evoked responses in neurosurgery. Front Pharmacol. 2014 Apr 14;5:74. doi: 10.3389/fphar.2014.00074. eCollection 2014. No abstract available.
PubMed 24782777Cabraja M, Stockhammer F, Mularski S, Suess O, Kombos T, Vajkoczy P. Neurophysiological intraoperative monitoring in neurosurgery: aid or handicap? An international survey. Neurosurg Focus. 2009 Oct;27(4):E2. doi: 10.3171/2009.7.FOCUS0969.
PubMed 19795951
Study at a glance
From the registry record, last updated by the sponsor on 23 Jun 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Physical Effects and Emotional Experiences of Intra-operative Neuro-monitoring (IONM)
- ClinicalTrials.gov ID
- NCT04443465
- Acronym / sponsor ID
- IONM / IRAS 239002
- Conditions
- Intraoperative Neurophysiological Monitoring, Complication, Intraoperative Complications, Postoperative Complications
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- King's College Hospital NHS TrustUniversity, hospital or other
- Study start
- 10 Oct 2018 (actual)
- Primary completion
- 10 Mar 2020 (actual)
- Study completion
- 10 Mar 2021 (estimated)
- First posted
- 23 Jun 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Resection of brain tumours forms a large proportion of work in brain surgery. One important aspect is to minimize damage to normal brain structures during this process. This improves patient outcomes and reduces complications. To identify normal brain structures from the abnormal tumours, the brain surgeons use a 'guidance' technique called intraoperative neuro-monitoring (IONM).
IONM uses various electrodes to observe spontaneous electrical activity of the brain or its reaction to a stimulus such as muscle contraction, light or sound. It is now becoming common practice for neurosurgeons to use this tool during brain and spinal surgery to provide a real-time feedback under anaesthesia to help them minimise injury to important and normal brain and spine structures.
IONM interpretation needs fulfilment of multiple preconditions and major modifications to the anaesthetic to reduce its inaccuracies. This invites added risks and complications such as awareness, convulsions and heart problems under anaesthesia. A team approach between the surgeon, anaesthetist and neurophysiologist (IONM specialist) is also crucial to obtain meaningful results. Therefore, the usefulness of this technique is still not perfect.
Although, benefits of IONM are obvious, information on associated complications and patient experience are not commonly found in the literature. Information on other effects such as hormonal balance and tumour recurrence are also scarce. In general, these aspects have little scientific exploration.
There are anecdotal reports of recurrent seizures during IONM leading to serious heart problems, teeth and tongue damage due to grinding and postoperative calf muscle injury necessitating further surgery to save limbs. Neither of these is in the literature including unorthodox treatments such as the use of cold saline to control IONM triggered fits.
This study is designed to observe complications and outcome and explore patient experiences following IONM in an observational capacity not interfering with the clinical management or treatment of these patients. The investigators intend to interview the participants after surgery, at a convenient time before leaving hospital to understand their views and experiences during and after surgery and their general progress in the following one year.
Detailed description
INTRODUCTION Intraoperative neuro-monitoring (IONM) is a 'SAT NAV' used by neurosurgeons to prevent injury to normal structures during brain and spinal surgery under anaesthesia. It involves the use of surface and implanted electrodes to observe spontaneous electrical activity of the brain or evoked responses to an electrical stimulus (motor, visual or auditory). This requires major modifications to the anaesthetic that provides lighter planes of anaesthesia with no muscle relaxation inviting added risks and complications such as awareness, seizures and cardiac events.
This cohort study over a period of one year will include a qualitative enquiry of patient experience and a quantitative evaluation of the immediate postoperative course and complications at 28 days and 1 year. It will explore the relatively unknown area of emotional experiences of participants under anaesthesia who undergo various types of neuro stimulation and related post-operative sequelae. The results are expected to assist improve patient experiences and outcomes.
BACKGROUND AND RATIONALE Resections of brain tumours constitute a significant proportion of work in neurosurgery. One important aspect is minimizing injury to normal neural structures during this process to improve outcomes of such operations and reduce complications. This involves intraoperative neuro-monitoring (IONM).
IONM uses surface and implanted electrodes to observe spontaneous electrical activity of the brain or evoked response to a motor, visual or auditory stimulus. It is now becoming common practice for neurosurgeons to use this tool during brain and spinal surgery to provide a real-time feedback under anaesthesia to help them minimise injury to critical and normal neural structures by 'mapping' normal from abnormal areas of the brain.
IONM interpretation needs fulfilment of multiple preconditions and major modifications to the anaesthetic to reduce its inaccuracies. This invites added risks and complications such as awareness, seizures and cardiac events. A team approach is also crucial to obtain meaningful results. Therefore, the utility of this technique is still evolving based on personal experiences and perceptions and the understanding between the surgeons, anaesthetists and neurophysiologists.
Although, benefits of IONM are obvious, data on associated post-operative morbidity and patient experience and complications are scarce. The data is also scarce on tumour recurrence or tumour behaviour following IONM guided neurosurgery. More precise excision may reduce tumour recurrence. On the other hand IONM related electrical stimulation may impose humoral effects on tumour behaviour. These aspects have little scientific exploration.
There are anecdotal reports of recurrent seizures during IONM leading to cardiac events such as asystole, teeth grinding and damage and tongue injury in the absence of a 'bite block' and postoperative calf muscle necrosis necessitating fasciotomies. Neither of these is in the literature including the unorthodox effective treatments used such as pouring 'cold' saline on the surface of the brain to control seizures.
The study will take place in a major neurosurgical centre in the UK that uses IONM. Therefore, the study population is vast for appropriate sampling and recruitment.
STUDY DESIGN This is an observational cohort study based on data retrieved from clinical notes and direct patient interview in hospital. The qualitative enquiry will address emotional aspects and the process experience. The quantitative survey will investigate morbidity (post-operative recovery, complications) and outcomes including mortality at 28 days and 1-year follow-up.
The eligible patients will be identified by the published elective neurosurgery lists and approached for informed consent before surgery at the time of preoperative assessment.
The anaesthetist or the surgeon directly involved with his/her clinical care will first approach the patient and subsequently introduced to the medical student for post-operative data collection. Their demographic data, disease data, and neurological assessment scores will be obtained from medical records. Direct patient interviews will be carried out by the investigators postoperatively, using a structured open questionnaire format. This activity will merge with the postoperative clinical rounds where possible.
All patients undergoing elective neurosurgery guided by IONM will be eligible for the study and recruited with informed consent. The exclusion criteria shall be aged less than 10 years, lack of informed consent and who are unable to communicate verbally.
A convenient sample of 50 is a realistic number of patients who can be recruited within a 3-month period at this centre. However, the qualitative enquiry may be stopped at an earlier time if the data collected is felt to be at the saturation point by the investigators. The participants shall be followed up at 28 days and 1-year post surgery.
Continuous data will be described and analysed based on their distribution, be it parametric or non-parametric. Dichotomous data will be described as number of patients/episodes and percentage.The patient experiences reported will be subjected to a thematic analysis following the principles of qualitative research grounded theory.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 10 years and older
- Sex
- All
- Age groups
- Child, Adult, Older adult
- Study population
- Adults and children aged 10 and above undergoing brain or spinal surgery with intra operative neurophysiological monitoring with intravenous anaesthesia
Key inclusion criteria (1 listed)
- All patients aged 10 and above undergoing elective neurosurgery guided by IONM will be recruited with informed consent.
Key exclusion criteria (1 listed)
- Lack of informed consent and who are unable to communicate verbally.-
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Experiences of participants who undergo intra-operative neurophysiological monitoring under anaesthesia
Time frame: 2 years
A qualitative study of patient experiences by thematic analysis
3 secondary outcomes
IONM related postoperative sequel during post surgical recovery in hospital
Time frame: 2 years
Mortality at 28 day and 1 year follow up
Time frame: 2 years
Morbidity at 28 days and 1 year follow up
Time frame: 2 years
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Jun 2020.
- Background: PubMed 22905324Stecker MM. A review of intraoperative monitoring for spinal surgery. Surg Neurol Int. 2012;3(Suppl 3):S174-87. doi: 10.4103/2152-7806.98579. Epub 2012 Jul 17.
- Background: PubMed 17342964Jameson LC, Sloan TB. Monitoring of the brain and spinal cord. Anesthesiol Clin. 2006 Dec;24(4):777-91. doi: 10.1016/j.atc.2006.08.002.
- Background: PubMed 24702618Arnold PM. Use of intraoperative monitoring in children. J Neurosurg Pediatr. 2014 Jun;13(6):589. doi: 10.3171/2013.9.PEDS13439. Epub 2014 Apr 4. No abstract available.
- Background: PubMed 2868172Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet. 1986 Feb 8;1(8476):307-10.
- Results publication: PubMed 17884710Jameson LC, Janik DJ, Sloan TB. Electrophysiologic monitoring in neurosurgery. Anesthesiol Clin. 2007 Sep;25(3):605-30, x. doi: 10.1016/j.anclin.2007.05.004.
- Results publication: PubMed 24782777Soghomonyan S, Moran KR, Sandhu GS, Bergese SD. Anesthesia and evoked responses in neurosurgery. Front Pharmacol. 2014 Apr 14;5:74. doi: 10.3389/fphar.2014.00074. eCollection 2014. No abstract available.
- Results publication: PubMed 19795951Cabraja M, Stockhammer F, Mularski S, Suess O, Kombos T, Vajkoczy P. Neurophysiological intraoperative monitoring in neurosurgery: aid or handicap? An international survey. Neurosurg Focus. 2009 Oct;27(4):E2. doi: 10.3171/2009.7.FOCUS0969.
- Individual participant dataSharing planned: Undecided. Anonymised qualitative and quantitative data
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Chulananda Goonasekera, PhD principal investigator
Kings College Hospital NHS Trust, London
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Intraoperative Neurophysiological Monitoring and Complication, run by King's College Hospital NHS Trust at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 23 Jun 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Experiences of participants who undergo intra-operative neurophysiological monitoring under anaesthesia (time frame: 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04443465, which also lists 7 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jun 2020.