Spinal Cord InjuryNCT01241630
Somato-sensory Reflex Arch in Spinal Cord Injury - Effect on Clinical Outcome
A study testing Somatosensory reflex arch (Xiao Procedure) in people with Spinal Cord Injury, run by University of Aarhus at 1 site in Denmark.
Trial summary
Spinal cord injury (SCI) usually affects young people and causes severe bowel and bladder dysfunction. Recently, the concept of a surgically created somat-sensory reflex arch for bladder dysfunction in SCI has been introduced. The concept is promising, not just for bladder but also for bowel dysfunction. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Spinal Cord Injury
- What is being tested?
- Somatosensory reflex arch (Xiao Procedure)
- Type of treatment
- Surgery or procedure
- How many people
- 10 participants
- Where
- 1 siteDenmark
- Study dates
- Nov 2009to Sep 2013
- Phase
- Interventional
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 18 years of age or above with motoric complete
- Spinal cord injury medullary level C4-L4
- Preserved Hamstring reflex (L5)
- Participation acceptance in verbal and writing
Who cannot join
- Respiratory dependent patient Baclofen pump Malignancy in the urinary tract, surgery on the urinary tract, urethral strictures Ileostomy, Colostomy or radiation towards the area Pregnancy, for men planning a pregnancy with their partner
Trial locations and contacts
1 site in 1 country.
About this study
Spinal cord injury (SCI) usually affects young people and causes severe bowel and bladder dysfunction. Recently, the concept of a surgically created somat-sensory reflex arch for bladder dysfunction in SCI has been introduced. The concept is promising, not just for bladder but also for bowel dysfunction. However, well designed studies need to be performed before recommending the procedure to a large number of patients worldwide. In this study we perform multidisciplinary studies providing necessary information about the clinical outcome of the somato-sensory reflex arch in adult SCI patients.
The hypothesis is as follows:
- In a "western setting" the somato-sensory reflex arch can be created in adult SCI patients with only minor morbidity and complications.
- Somato-sensory reflex arch reduces bladder and bowel symptoms in SCI patients.
Read the detailed description
Introduction:
Spinal cord injury has a profound impact on the lives of those affected. Quality of life is restricted not only by immobility but also by severe neurogenic bladder and bowel dysfunction. For example, 66% of SCI patients have to empty their rectum digitally, 75% suffer from faecal incontinence and 9% spend more than 60 minutes each time they defecate. Neurological impairment due to SCI is permanent and the average age at injury is only 28 years. The longevity of individuals with SCI is approaching that of the general population and, accordingly, most patients have to live for several decades with severe bladder and bowel symptoms. It is estimated that the number of individuals with SCI in Denmark is 3.000 and each year 10.000 persons in the European Union sustain a SCI. Even though clean intermittent catheterization has successfully reduced mortality due to urinary tract infections or reflux and though several new treatment modalities for neurogenic bowel dysfunction have been introduced, both bladder and bowel dysfunction still rank among the top three causes of impairment of quality of life after SCI.
Somato-sensory reflex arch:
The concept was pioneered by professor Xiao. Animal studies and basic clinical research were performed in the United States and later human clinical studies have been done in Wuhan, China. The surgical procedure principle can briefly be summarized as follows:
All spinal nerves have an anterior efferent root and a posterior afferent root. For the somato-sensory reflex arch (or "Xiao procedure") the posterior (afferent or sensory) root of the 5th lumbar nerve (L5) is kept while the anterior root is cut and anastomosed to the anterior root of a lower segment, usually the third sacral segment (S3). Thereby, a new reflex arch has been created from the skin of the leg through the sensory part of L5 to the spinal cord and further through the anastomosis via S2 or S3 to the bladder and bowel. Strong stimuli at the L5 dermatome, i.e. scratching or electrical stimulation, will then initiate voiding (6,7). Effects of the somato-sensory reflex arch on neurogenic bowel dysfunction have not been studied, but clinical experience indicates that bowel management is substantially facilitated.
The Xiao procedure introduces a completely new concept for management of spinal cord lesions and it has been greeted with optimism worldwide. The number of patients operated in China alone is now more than 3.000 and centres in the United States, Germany and Israel have introduced or modified it. Furthermore, centres in Australia, Finland and Denmark plan to introduce it within the present year. There are, however, serious concerns that need to be addressed:
Clinical follow-up has only been done in very few patients and physiological studies after the procedure are equally few and small.
In spite of the very large number of patients operated in China logistic or cultural factors have prohibited effective follow-up.
A minor improvement in bladder and bowel function may be important to a Chinese patient without access to other treatment but it is unknown whether the Xiao procedure will be an advantage to patients in a western healthcare system.
The mode of action of the somato-sensory reflex arch is very incompletely studied and the mode of action on bowel function not studied at all.
Before the widespread use of somato-sensory reflex arch we find it of utmost importance that well designed studies with validated or even objective endpoints are performed. Results of such studies will have an international impact in either defining indications for a completely new treatment principle or, otherwise, in preventing the widespread use of an ineffective treatment.
Hypotheses:
In March 2009 the core members of our multidisciplinary study team went on a study tour to Wuhan, China. In Wuhan a staggering number of 600 patients had the somato-sensory reflex arch procedure performed in 2008. Based on experience from our visit we pose the following hypotheses:
- In a "western setting" the somato-sensory reflex arch can be created in adult SCI patients with only minor morbidity and complications.
- Somato-sensory reflex arch reduces bladder and bowel symptoms in SCI patients.
Patients and Methods:
Spinal cord injured patients
Internationally, two indications for the somato-sensory reflex arch are emerging:
Adult patients with bladder dysfunction due supraconal SCI (above the conus medullaris) and Children with bladder dysfunction due to spinal bifida. Most children with spinal bifida have motor incomplete lesions and, accordingly, the surgical procedure carries a risk of long-lasting or even permanent loss of motor function - typically loss of dorsiflexion of the foot. Whether results from the procedure justify that risk remains to be determined. In contrast, patients with motor complete supraconal SCI, and thereby complete loss of voluntary muscle function below the level of injury, do not run that risk. Therefore, it has been decided that patients in group a) above will be offered the procedure at the Department of Neurosurgery NK, AUH. Initially, 20 patients will undergo the procedure. As the method is new, surgery and follow-up will be performed under strict monitoring with emphasis on neurophysiologic testing and potential complications. Approval will be obtained from the Ethics Committee, patients will be very carefully informed by the neurosurgeon (Dorte Clemmensen) and informed consent will be signed.
Surgical procedure:
The relatively minor surgical procedure has been described in previously. In summary: A hemilaminectomy of L5-S1 is performed. By means of neurophysiology testing the 5th lumbar root and 2nd or 3rd sacral roots are identified on one side. The perineurium is opened and the motor roots are separated from the sensory. The motor roots are transsected and a microanastomosis is created between L5 and S2 or S3. After surgery sprouting occurs and after 12-18 months the reflex arch is functional. Time till clinical effect is therefore also 12-18 months. The advantage of the procedure is that it is performed through a hemilaminectomy of only two segments and the surgical stress in relatively small. The patients are expected to be in their habitual condition within 48 hours.
Post surgical monitoring:
Through informal contacts it has been agreed that complications and basic functional results from three centres about to adopt the procedure (Melbourne, Australia; Helsinki, Finland; and Aarhus, Denmark) will be recorded in a standardized way. Preliminary principles for assessment have been agreed upon and other centres introducing the procedure in the future will be invited to participate. This will allow comparison of results between centres.
Study A). Detailed assessment of functional results of the somato-sensory reflex arch To patients the main concern is whether the procedure is safe and reduces symptoms. Detailed and internationally accepted evaluation forms for adult SCI patients have recently been developed. The so called International Spinal Cord Injury Data Sets have been endorsed by the International Spinal Cord Organisation (ISCoS) and the American Spinal Cord Association (ASIA). Information within the data sets are mainly symptom based but for lower urinary tract function urodynamic assessment is included and for bowel function radiographically determined colorectal transit time is included. From the bowel function data sets the most commonly used scores for bowel dysfunction, including the Neurogenic Bowel Dysfunction Score, developed at our unit, can be computed.
Patients undergoing the surgical procedure will be assessed using the basic and extended lower urinary tract data sets and the bowel function data sets before surgery and 18 months after. Before
Based on the investigations above, we aim at publishing the following sub-studies:
A1). Prospective study of urodynamic function and bladder symptoms before and after somato-autonomic reflex arch in spinal cord injury patients.
A2). Prospective study of colorectal symptoms before and after somato-autonomic reflex arch in spinal cord injury patients.
A3). Prospective study of colorectal transit times and rectal wall properties after somato-autonomic reflex arch in spinal cord injury patients.
- Conditions
- Spinal Cord Injury
- Being tested
- Somatosensory reflex arch (Xiao Procedure)
- Keywords
- Somato-sensory reflex arch, Spinal cord injury, Xiao Procedure
- Medical subject headings
- Spinal Cord Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Somatosensory reflex arch (Xiao Procedure)Procedure or surgery
Also called Somato-sensory reflex arch, Artificial somato-sensory reflex arch
Cross over surgery. Proximal part of L5 Ventral root is anastomosed to distal part of ventral root of S2 or S3 producing a somato-sensory reflex arch
What is being measured
The primary outcome is the main question the study is designed to answer.
Urodynamic function and bladder symptoms before and after somato-autonomic reflex arch in spinal cord injury patients
Prospective study of urodynamic function and bladder symptoms before and after somato-autonomic reflex arch in spinal cord injury patients.
Measured: 2013 (anticipated)
Secondary outcomes (3)
Colorectal symptoms before and after somato-autonomic reflex arch in spinal cord injury patients
Prospective study of colorectal symptoms before and after somato-autonomic reflex arch in spinal cord injury patients.
Measured: 2013 (anticipated)
Colorectal transit times and rectal wall properties after somato-autonomic reflex arch in spinal cord injury patient
Prospective study of colorectal transit times and rectal wall properties after somato-autonomic reflex arch in spinal cord injury patients.
Measured: 2013 (anticipated)
Effect of quality of Life after somato-autonomic reflex arch in spinal cord injury patient
Effect of quality of Life after somato-autonomic reflex arch in spinal cord injury patient
Measured: 2013 (anticipated)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Nov 2010 (estimated)
- Study startNov 2009
- Primary completionSep 2013
- Study completionSep 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Spinal Cord InjuryStudies of the same condition, open and under way.
- More trials run by University of AarhusThe 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Aarhus
- Sponsor type
- University, hospital or other
- Collaborators
- Lundbeck Foundation
- Responsible party
- Sponsor
- Investigators
- Klaus Krogh, MD,PhD, DmSc, Principal investigator, Aarhus University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01241630
- Sponsor's protocol ID
- M-20090113 - 2
- Status last verified
- Oct 2012
- First submitted
- 8 Nov 2010
- Last updated
- 12 May 2014
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 12 May 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Somato-sensory Reflex Arch in Spinal Cord Injury - Effect on Clinical Outcome
- ClinicalTrials.gov ID
- NCT01241630
- Acronym / sponsor ID
- M-20090113 - 2
- Conditions
- Spinal Cord Injury
- Keywords
- Somato-sensory reflex arch, Spinal cord injury, Xiao Procedure
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 10 participants (actual)
- Lead sponsor
- University of AarhusUniversity, hospital or other
- Collaborators
- Lundbeck Foundation
- Study start
- Nov 2009
- Primary completion
- Sep 2013 (actual)
- Study completion
- Sep 2013 (actual)
- First posted
- 16 Nov 2010 (estimated)
- 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.
Spinal cord injury (SCI) usually affects young people and causes severe bowel and bladder dysfunction. Recently, the concept of a surgically created somat-sensory reflex arch for bladder dysfunction in SCI has been introduced. The concept is promising, not just for bladder but also for bowel dysfunction. However, well designed studies need to be performed before recommending the procedure to a large number of patients worldwide. In this study we perform multidisciplinary studies providing necessary information about the clinical outcome of the somato-sensory reflex arch in adult SCI patients.
The hypothesis is as follows:
- In a "western setting" the somato-sensory reflex arch can be created in adult SCI patients with only minor morbidity and complications.
- Somato-sensory reflex arch reduces bladder and bowel symptoms in SCI patients.
Detailed description
Introduction:
Spinal cord injury has a profound impact on the lives of those affected. Quality of life is restricted not only by immobility but also by severe neurogenic bladder and bowel dysfunction. For example, 66% of SCI patients have to empty their rectum digitally, 75% suffer from faecal incontinence and 9% spend more than 60 minutes each time they defecate. Neurological impairment due to SCI is permanent and the average age at injury is only 28 years. The longevity of individuals with SCI is approaching that of the general population and, accordingly, most patients have to live for several decades with severe bladder and bowel symptoms. It is estimated that the number of individuals with SCI in Denmark is 3.000 and each year 10.000 persons in the European Union sustain a SCI. Even though clean intermittent catheterization has successfully reduced mortality due to urinary tract infections or reflux and though several new treatment modalities for neurogenic bowel dysfunction have been introduced, both bladder and bowel dysfunction still rank among the top three causes of impairment of quality of life after SCI.
Somato-sensory reflex arch:
The concept was pioneered by professor Xiao. Animal studies and basic clinical research were performed in the United States and later human clinical studies have been done in Wuhan, China. The surgical procedure principle can briefly be summarized as follows:
All spinal nerves have an anterior efferent root and a posterior afferent root. For the somato-sensory reflex arch (or "Xiao procedure") the posterior (afferent or sensory) root of the 5th lumbar nerve (L5) is kept while the anterior root is cut and anastomosed to the anterior root of a lower segment, usually the third sacral segment (S3). Thereby, a new reflex arch has been created from the skin of the leg through the sensory part of L5 to the spinal cord and further through the anastomosis via S2 or S3 to the bladder and bowel. Strong stimuli at the L5 dermatome, i.e. scratching or electrical stimulation, will then initiate voiding (6,7). Effects of the somato-sensory reflex arch on neurogenic bowel dysfunction have not been studied, but clinical experience indicates that bowel management is substantially facilitated.
The Xiao procedure introduces a completely new concept for management of spinal cord lesions and it has been greeted with optimism worldwide. The number of patients operated in China alone is now more than 3.000 and centres in the United States, Germany and Israel have introduced or modified it. Furthermore, centres in Australia, Finland and Denmark plan to introduce it within the present year. There are, however, serious concerns that need to be addressed:
Clinical follow-up has only been done in very few patients and physiological studies after the procedure are equally few and small.
In spite of the very large number of patients operated in China logistic or cultural factors have prohibited effective follow-up.
A minor improvement in bladder and bowel function may be important to a Chinese patient without access to other treatment but it is unknown whether the Xiao procedure will be an advantage to patients in a western healthcare system.
The mode of action of the somato-sensory reflex arch is very incompletely studied and the mode of action on bowel function not studied at all.
Before the widespread use of somato-sensory reflex arch we find it of utmost importance that well designed studies with validated or even objective endpoints are performed. Results of such studies will have an international impact in either defining indications for a completely new treatment principle or, otherwise, in preventing the widespread use of an ineffective treatment.
Hypotheses:
In March 2009 the core members of our multidisciplinary study team went on a study tour to Wuhan, China. In Wuhan a staggering number of 600 patients had the somato-sensory reflex arch procedure performed in 2008. Based on experience from our visit we pose the following hypotheses:
- In a "western setting" the somato-sensory reflex arch can be created in adult SCI patients with only minor morbidity and complications.
- Somato-sensory reflex arch reduces bladder and bowel symptoms in SCI patients.
Patients and Methods:
Spinal cord injured patients
Internationally, two indications for the somato-sensory reflex arch are emerging:
Adult patients with bladder dysfunction due supraconal SCI (above the conus medullaris) and Children with bladder dysfunction due to spinal bifida. Most children with spinal bifida have motor incomplete lesions and, accordingly, the surgical procedure carries a risk of long-lasting or even permanent loss of motor function - typically loss of dorsiflexion of the foot. Whether results from the procedure justify that risk remains to be determined. In contrast, patients with motor complete supraconal SCI, and thereby complete loss of voluntary muscle function below the level of injury, do not run that risk. Therefore, it has been decided that patients in group a) above will be offered the procedure at the Department of Neurosurgery NK, AUH. Initially, 20 patients will undergo the procedure. As the method is new, surgery and follow-up will be performed under strict monitoring with emphasis on neurophysiologic testing and potential complications. Approval will be obtained from the Ethics Committee, patients will be very carefully informed by the neurosurgeon (Dorte Clemmensen) and informed consent will be signed.
Surgical procedure:
The relatively minor surgical procedure has been described in previously. In summary: A hemilaminectomy of L5-S1 is performed. By means of neurophysiology testing the 5th lumbar root and 2nd or 3rd sacral roots are identified on one side. The perineurium is opened and the motor roots are separated from the sensory. The motor roots are transsected and a microanastomosis is created between L5 and S2 or S3. After surgery sprouting occurs and after 12-18 months the reflex arch is functional. Time till clinical effect is therefore also 12-18 months. The advantage of the procedure is that it is performed through a hemilaminectomy of only two segments and the surgical stress in relatively small. The patients are expected to be in their habitual condition within 48 hours.
Post surgical monitoring:
Through informal contacts it has been agreed that complications and basic functional results from three centres about to adopt the procedure (Melbourne, Australia; Helsinki, Finland; and Aarhus, Denmark) will be recorded in a standardized way. Preliminary principles for assessment have been agreed upon and other centres introducing the procedure in the future will be invited to participate. This will allow comparison of results between centres.
Study A). Detailed assessment of functional results of the somato-sensory reflex arch To patients the main concern is whether the procedure is safe and reduces symptoms. Detailed and internationally accepted evaluation forms for adult SCI patients have recently been developed. The so called International Spinal Cord Injury Data Sets have been endorsed by the International Spinal Cord Organisation (ISCoS) and the American Spinal Cord Association (ASIA). Information within the data sets are mainly symptom based but for lower urinary tract function urodynamic assessment is included and for bowel function radiographically determined colorectal transit time is included. From the bowel function data sets the most commonly used scores for bowel dysfunction, including the Neurogenic Bowel Dysfunction Score, developed at our unit, can be computed.
Patients undergoing the surgical procedure will be assessed using the basic and extended lower urinary tract data sets and the bowel function data sets before surgery and 18 months after. Before
Based on the investigations above, we aim at publishing the following sub-studies:
A1). Prospective study of urodynamic function and bladder symptoms before and after somato-autonomic reflex arch in spinal cord injury patients.
A2). Prospective study of colorectal symptoms before and after somato-autonomic reflex arch in spinal cord injury patients.
A3). Prospective study of colorectal transit times and rectal wall properties after somato-autonomic reflex arch in spinal cord injury patients.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 18 years of age or above with motoric complete
- Spinal cord injury medullary level C4-L4
- Preserved Hamstring reflex (L5)
- Participation acceptance in verbal and writing
Key exclusion criteria (1 listed)
- Respiratory dependent patient Baclofen pump Malignancy in the urinary tract, surgery on the urinary tract, urethral strictures Ileostomy, Colostomy or radiation towards the area Pregnancy, for men planning a pregnancy with their partner
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Somatosensory reflex arch (Xiao Procedure)Also: Somato-sensory reflex arch, Artificial somato-sensory reflex archCross over surgery. Proximal part of L5 Ventral root is anastomosed to distal part of ventral root of S2 or S3 producing a somato-sensory reflex arch | Procedure or surgery | – |
Primary outcome
Urodynamic function and bladder symptoms before and after somato-autonomic reflex arch in spinal cord injury patients
Time frame: 2013 (anticipated)
Prospective study of urodynamic function and bladder symptoms before and after somato-autonomic reflex arch in spinal cord injury patients.
3 secondary outcomes
Colorectal symptoms before and after somato-autonomic reflex arch in spinal cord injury patients
Time frame: 2013 (anticipated)
Colorectal transit times and rectal wall properties after somato-autonomic reflex arch in spinal cord injury patient
Time frame: 2013 (anticipated)
Effect of quality of Life after somato-autonomic reflex arch in spinal cord injury patient
Time frame: 2013 (anticipated)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 May 2014.
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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.
Klaus Krogh, MD,PhD, DmSc principal investigator
Aarhus University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Somatosensory reflex arch (Xiao Procedure) in people with Spinal Cord Injury, run by University of Aarhus at 1 site in Denmark.
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 4 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: finished, as of the sponsor's last update on 12 May 2014. 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 Denmark. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Urodynamic function and bladder symptoms before and after somato-autonomic reflex arch in spinal cord injury patients (time frame: 2013 (anticipated)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 12 May 2014.