Acupuncture Clinical Trial
Official title:
Effect of Perioperative Electroacupuncture After Gastrectomy for Gastric Cancer Patients on Rapid Rehabilitation: A Randomized Clinical Trial
Evaluate the effect of Perioperative Electroacupuncture on rapid rehabilitation for the gastric cancer patients after gastrectomy .
The trial is funded by Cancer Foundation of China. The trial is prepared to be registered on
the clinicaltrail.gov. Quality assurance plan: every participant is enrolled or excluded by
two practiced investigators. And two investigators participated in all steps of the trail,
including the record of the data, and the investigators will compare the data. If the data is
consistent, the investigators would record the data; if not, the data would be checked and
decided by the two investigators. All the steps and data are site monitored and audited by
the workers of research and financial department of National Cancer Center/ Cancer Hospital,
Chinese Academy of Medical Sciences. Data check: the investigators compare data entered into
the registry against predefined rules for range or consistency with other data fields in the
registry. Source data verification to assess the accuracy, completeness, or
representativeness of registry data by comparing the data to external data sources, including
medical records and electronic case report forms. Data dictionary that contains detailed
descriptions of each variable used by the registry, including the source of the variable,
coding information, and normal ranges if relevant.
Standard Operating Procedures to address registry operations and analysis activities, such as
participants recruitment, data collection, data management, data analysis, reporting for
adverse events, and change management. All registry operations would be done according to
specific steps, and by two practiced investigators. Sample size assessment to specify the
number of participants or participant years necessary to demonstrate an effect. According to
the formula to differ advantages and disadvantages, the investigators need at least 70
participants to take part in the trail.
The investigators can recruit about 35 participants every year according to previous
experiences, so the investigators should recruit at least for two years. Plan for missing
data: the investigators would collect as much data as possible, and the investigators exclude
the participants who cannot cooperate on recruitment. And the investigators manage situations
according to statistical principles where variables are reported as missing, unavailable,
"non-reported," uninterpretable, or considered missing because of data inconsistency or
out-of-range results. Statistical analysis plan: Kaplan-Meier method would be used to analyze
the difference of survival time between the two groups, and the local control rate of the two
groups would be compared by chi square test. Statistical analyses would be performed by using
IBM SPSS Statistics(version 20; IBM, Chicago, USA). The level of significance is defined as P
< 0.05.
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