- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04941859
Medicine Acuity Patching Combined Massage in the Treatment of Patients With Acute Poisoning
June 18, 2021 updated by: Second Affiliated Hospital, School of Medicine, Zhejiang University
The Study of Chinese Medicine Acuity Patching Combined Massage in the Treatment of Patients With Acute Poisoning and Stomach Washing
This topic in western medicine combined on the basis of gastric lavage therapy in patients with acute poisoning acupoint sticking of traditional Chinese medicine and acupuncture point massage treatment, aims to smoothly accelerate cleaning and discharge poison, increase the poisoning patients rescue success rate, improve patient quality of life, for the clinical treatment of acute poisoning provides a new method of TCM nursing, to further exert TCM nursing characteristics.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
With the rapid development of national economy, people's exposure to a variety of chemicals, drugs and other opportunities to increase, the types of substances causing poisoning tend to be diversified, acute poisoning frequently occur.
Data showed that in some regions of China, poisoning cases accounted for 2.7%~ 3.6% of the patients admitted to the emergency department in the same period , and 8.3 % of the patients rescued in the emergency department in the same period , and its fatality rate was higher than the total fatality rate in the emergency department .
The incidence of poisoning was 18/100,000 in urban residents and 69.22/100,000 in rural areas, accounting for 10.7% of all deaths.
Poisoning incident is an important part of national public health emergency management.
According to the statistics of China's Ministry of Health in 2013, poisoning has entered the top five major causes of death in China, and the number of acute poisoning cases has been increasing year by year .
The diagnosis and treatment of acute poisoning and the effective and rapid treatment have become an important task for emergency clinical workers.
Study Type
Interventional
Enrollment (Anticipated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: minfei yang
- Phone Number: +86 13757118252
- Email: 2200056@zju.edu.cn
Study Locations
-
-
Zhejiang
-
Hanzhou, Zhejiang, China, 310000
- Recruiting
- 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China
-
Contact:
- minfei yang
- Phone Number: +8613757118252
- Email: 2200056@zju.edu.cn
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 60 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients with oral acute poisoning who were first diagnosed in our hospital and completed gastric lavage;
- The skin of umbilical cord and bilateral Zusanli acupoints had no injury, scar, rash and other skin diseases.
- The patient or the patient's family member signed the informed consent and expressed their willingness to receive treatment.
Exclusion Criteria:
- Patients with severe conditions requiring cardiopulmonary resuscitation or with severe trauma or multiple injuries;
- Patients with heart, brain, liver, kidney and hematopoietic system diseases and other serious primary diseases;
- Patients with a history of gastrointestinal diseases (such as postoperative cancer, intestinal obstruction, and large intestinal polyps) that affect gastrointestinal emptying;
- Failing to receive treatment according to regulations or taking poison again during hospitalization and unable to judge the curative effect.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental group
Patients in the experimental group were treated with acupoint application combined with acupoint massage on the basis of standard treatment for acute poisoning.
When the patient began to launder the stomach, the acupoint was applied to Shenque (umbilical).
After the end of the gastric launder, Shenque acupoint and Zusanli diarrhea method (referring to counterclockwise and strong stimulation) were massaged for 15 minutes, and the massage frequency was Q8H.
|
Patients in the experimental group were treated with acupoint application combined with acupoint massage on the basis of standard treatment for acute poisoning.
When the patient began to launder the stomach, the acupoint was applied to Shenque (umbilical).
After the end of the gastric launder, Shenque acupoint and Zusanli diarrhea method (referring to counterclockwise and strong stimulation) were massaged for 15 minutes, and the massage frequency was Q8H.
|
|
No Intervention: control group
The treatment plan of control group was carried out according to the diagnosis and treatment standard of acute poisoning.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
complications
Time Frame: one year
|
Incidence of complications within 24 hours of admission: including nausea, vomiting, and abdominal pain
|
one year
|
|
Time of first bowel movement
Time Frame: through study completion, an average of 1 year
|
Time of first bowel movement
|
through study completion, an average of 1 year
|
|
patient duration of hospital stay
Time Frame: through study completion, an average of 1 year
|
patient duration of hospital stay
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: minfei yang, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 8, 2021
Primary Completion (Anticipated)
December 31, 2021
Study Completion (Anticipated)
December 31, 2021
Study Registration Dates
First Submitted
June 18, 2021
First Submitted That Met QC Criteria
June 18, 2021
First Posted (Actual)
June 28, 2021
Study Record Updates
Last Update Posted (Actual)
June 28, 2021
Last Update Submitted That Met QC Criteria
June 18, 2021
Last Verified
June 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-0023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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