Spinal Cord Injury Clinical Trial
Official title:
Pre-and In-hospital First Aid Programs and Specifications for Spine and Spinal Cord Injury in Beijing of China: a Prospective, Multicenter, Case Series Trial
To establish a spine injury and spinal cord injury (SCI) treatment database; to complete pre- and in-hospital evaluation of spine injury and SCI, develop and optimize first aid procedures, form pre-and in-hospital standardized training program for the treatment of spine injury and SCI; to develop first aid guidelines and establish an evaluation and treatment system for early surgery, as far as possible to save the spinal cord function and reduce the degree of disability; to form expert consensus on acute SCI and "green channel" patterns, will be promoted in hospitals in Beijing and other cities of China, so as to improve the level of first aid treatment of acute spine injury and SCI in Chinese cities, and to reduce the occurrence of secondary injury and severe dysfunction due to improper treatment.
This is a prospective, multicenter, non-randomized controlled trial. The target population
consists of 200 acute spinal cord injury patients undergoing pre-hospital treatment in the
Beijing Emergency Medical Center and Beijing Red Cross Emergency Rescue Center, and
receiving in-hospital treatment in the Peking University People's Hospital, Peking
University Third Hospital, Beijing Friendship Hospital Affiliated to Capital Medical
University, Chaoyang Hospital Affiliated to Capital Medical University, and Chinese PLA
General Hospital, China.
History and current related studies Acute spinal cord injury (SCI) as a clinical common
disease is the difficulty of clinical treatment, and frequently occurs in young adults. The
incidence of acute SCI is 30-40/million people in Europe and USA, but 60.2/million people in
Beijing of China. The complete SCI is very dangerous, and there is no effective medical
therapy. At present, the effective treatment of acute SCI should be the first aid and
advanced rehabilitation.
24 hours is the best time to rescue spinal cord function after SCI, especially 3-8 hours
after injury is the golden opportunity. A large dose of hormone therapy in the 3-8 hours
after injury can reduce secondary injury, thereby reducing the degree of SCI. 24 hours after
injury, early surgery for relieving spinal cord compression can significantly improve the
recovery of spinal cord function. Timely and properly pre-hospital first aid, quick hospital
admissions and assessment, and timely surgery are essential for the rescue of spinal cord
function. Patients with incomplete SCI can be completely injured and lose the possibility of
recovery of spinal cord function due to improper first aid or untimely treatment. Complete
SCI will cause more severe injury due to improper treatment. It may be difficult to make up
for surgery or rehabilitation training. A sound and rapid treatment system is the basis for
improving the treatment level of SCI, but we still lack of this kind of system in China.
In Beijing of China, pre-hospital treatment can be done by Beijing Emergency Medical Center
(120 first aid system) and Beijing Red Cross Hospital (999 first aid system). While
cooperating with each other, it is also faced with different mechanisms, different treatment
patterns and overlapping treatment regions. As for the in-hospital treatment, Beijing has a
large number of high-level hospitals, but these hospitals are overcrowding. There is no SCI
treatment specialist or professional hospital in Beijing City, so treatment basically relies
on various general hospitals. In pre-hospital first aid and in-hospital treatment of Beijing
City, the medical information transfer is not smooth; the treatment process is separated,
and it lacks of standardized treatment. The ability and level of medical personnels are not
consistent, the technology is backward, and there is lack of professional training. Thus,
the vast majority of patients with SCI cannot be treated within the optimal treatment time
after injury. It is also an important cause of higher mortality and disability in SCI
patients in China compared with the developed countries.
In 2006, Professor Bao-guo Jiang, director of the Department of Orthopedics, Peking
University People's Hospital, led the establishment of the Traffic Medicine Center of Peking
University, involving Peking University People's Hospital, School of Public Health of Peking
University, Peking University First Hospital, Peking University Third Hospital, Beijing
Traffic Management Bureau, and Beijing Emergency Medical Center in China. Reviewed by the
Health and Family Planning Commission, the "National Center for Severe Trauma Training" was
set up in 2015, and Bao-guo Jiang served as the director of the center. The Traffic Medicine
Center and two emergency centers in Beijing have cooperated for many years, and established
an epidemiological database for the treatment of severe trauma and the linkage mechanism of
pre-hospital and in-hospital. The treatment of spine injury and SCI is one of important
contents for treating severe trauma. With this center as a platform, the database of SCI
patients can be specialized; a unified standardized and rapid treatment can be carried out
in many participating medical units using the linkage mechanism with the emergency centers;
a high level of scientific research can be carried out, and a series of studies can be
started, concerning SCI epidemiology, treatment procedures and improvement in treatment
effect. Simultaneously, the standardized training for pre-hospital and in-hospital first aid
care personnel in each research center and hospital can be completed.
For nonstandard treatment process and path and poor information exchange, incoherent
pre-hospital care and in-hospital treatment, lack of professional training for treatment
personnel, and uneven comprehensive hospital treatment capacity, this trial aims to
formulate the standards for the treatment of spine injury and SCI through a standardized
multicenter study so as to improve the level of SCI treatment and to reduce the mortality
and disability of SCI patients in Beijing, China.
Statistical analysis
1. Statistical analysis will be performed using SPSS 19.0 software (IBM, Armonk, NY, USA)
2. Measurement data will be expressed as the case number (missing number), mean, median,
standard deviation, first quartile, third quartile, maximum, and minimum. The 95%
confidence interval of the rate will be calculated.
3. Count data will be expressed as the frequency and relative number. The 95% confidence
interval of the rate will be calculated.
4. Normally or non-normally distributed measurement data will be analyzed using paired
t-test or Wilcoxon signed rank test.
5. Count data will be analyzed using Chi-square test or Fisher exact test. Ranked data
will be analyzed using Wilcoxon signed rank test.
Sample size calculation In accordance with previous SCI treatment conditions in
participating units, we will recruit 200 cases.
Data management
1. The database will be constructed and maintained by Peking University People's Hospital.
According to the data characteristics of the research program, the main researcher will
draft detailed data management and statistical plans, including data quality audit,
construct corresponding electronic database, completely and accurately input all
expected data.
2. Each participating unit will be responsible for filling in the database of their
subjects.
3. The computer program combined with the manual method will be used to check the
consistency and logicality of the data.
4. Any questions will be answered by the person in charge of the project and the main
staff, and returned to the data management center, and then the data manager will
modify and update the database. All inspection procedures need to be repeated several
times until there is no doubt. All changes and updates are required for recording and
filing. It is strictly forbidden to use correction fluid or correction tape.
5. All researchers are required to ensure that the data recorded in the case report forms
are authentic.
Auditing
1. Peking University People's Hospital will organize training sessions before the study
and conduct unified training for all the participants. A person, as a coordinator, will
coordinate the whole research, prepare a research brief, regularly announce the
progress of the study, and solve the problems in the study.
2. The responsible person will hold a regular meeting, summarize the work, communicate,
correct the problem, and make a request.
3. In order to follow the Guidelines for Good Clinical Practice, we will set up a regular
visit to each center to ensure compliance with research programs, Good Clinical
Practice and related laws.
Quality control and management
1. In order to implement the research plan, it is necessary to hold the project launch
meeting of the heads of the participating units so as to carry out unified training for
the implementation of the project plan, and for the record and assessment.
2. The heads of the participating units will train specific operators on programs,
procedures, and instructions, develop training programs and manuals to ensure that the
team members are familiar with and grasp the relevant contents before the trial.
3. The inspector is responsible for ensuring the smooth progress of the trial, controls
the whole process, and deals with emergencies.
4. Each participating unit will perform its duties, strictly follow the clinical trial
program, and adopt standard operating procedures. Grading of quality-control staffs
will be set up; different grades of staffs will be responsible for different parts of
work, which will be inspected by the superior staff to ensure that the data will be
input in the database system within 24 hours after the incident and to ensure the
authenticity and validity.
5. A new team member will be trained, concerning project plan and process, and timely
trained, concerning the updated content/process or content that needs to be
re-emphasized.
6. Standard operation procedure will ensure smooth handover if necessary.
7. The arbitrator will guarantee the rights of each participating unit, make sure true,
accurate, complete and correct data record and report, and ensure that the research
follows the relevant laws and regulations. The number of visits of the arbitrator will
meet the needs of quality control. The arbitrator after each visit will inform the
project leader the inspection results.
8. Quality controller of each region will carry out internal inspection on scale filling
weekly according to the requirements.
9. According to the training program, the leader of each region will submit the results,
statements, and a summary report quarterly to the research group. The research group
will timely adjust the protocol according to the report.
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