- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05379660
Effects of TEAS on Postoperative Recovery of Intestinal Function in Children Undergoing Laparoscopic Appendectomy
May 17, 2022 updated by: Xian Children's Hospital
Effects of Transcutaneous Electrical Acupoint Stimulation on Postoperative Recovery of Intestinal Function in Children Undergoing Laparoscopic Appendectomy
With the development of surgical techniques, laparoscopic appendectomy has become a standard therapeutic procedure for acute appendicitis in many hospitals in recent years, which is considered as an effective and safe treatment option in children.
Even so, patients still experience gastrointestinal dysfunction after surgery, which is one of the most common complications in patients who have undergone major abdominal surgery.
The application of laparoscopy reduces trauma in some degree, however, postoperative nausea and vomiting (PONV), abdominal distension, fart, and delayed bowel movement caused by postoperative gastrointestinal dysfunction(PGD), severely disturb patients and seriously affect the quality of patients' postoperative recovery.
Previous studies have shown that the incidence of PGD can be as high as 10%-30%.
For PGD, the main treatment options include the use of gastric dynamics promoting drug, non-steroidal anti-inflammatory drug, gastrointestinal (GI) decompression, nutritional support, and so forth.
However, the effect of these treatments is limited, and there are varying degrees of adverse reactions, which indirectly leads to the low satisfaction of patients.
Acupuncture is a form of traditional Chinese medicine and has unique advantages in the treatment of PGD, which have gradually obtained more acceptance from physicians as an alternative therapy.
While transcutaneous electrical acupoint stimulation (TEAS) is one of the acupuncture-related technologies and can allow for accurate control of stimulation parameters.
For this reason, it is helpful for quantitative research and widely practiced in China.
Many studies have shown that TEAS combining with anesthetics can significantly enhance the analgesic effect and reduce the dosage of anesthetics, and can offer certain beneficial effects, such as alleviating preoperative anxiety and reducing postoperative pain and PONV by lessening need for anesthetic usage.
It also has been found to help protect the brain, heart and other tissues, with positive benefits for gastrointestinal function by regulating vasoactive intestinal peptide levels.
In practice, however, the current TEAS study focused on adults,with relatively little research on their use in children.
Because of that, we applied TEAS for use in our study to observe the effect of TEAS in children's laparoscopic surgery and explore its possible mechanism.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
200
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: Bin Hi Wu
- Phone Number: +8618092695276
- Email: 1922703776@qq.com
Study Contact Backup
- Name: Fang Li Yang
- Phone Number: +8613572190398
- Email: yanglf@fmmu.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
4 years to 14 years (CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- American Society of Anesthesiologists grade I&II,16kg/m2 ≤BMI≤30kg/m2, undergoing laparoscopic appendectomy
Exclusion Criteria:
- previous history of gastrointestinal surgery or abnormal anesthesia recovery, allergy, broken and infection skin at and around the related points, long-term use of analgesic and sedative drugs, presence of severe systemic disease,and the patients drop out or are unable to complete a full follow-up for any reason
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: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: QUADRUPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: T1 treatment group
TEAS initiates at 30 minutes before induction and lasts for 30 minutes
|
Basing on the theory of traditional Chinese medicine, bilateral Zusanli (ST 36), Shangjuxu (ST 37) and Sanyinjiao (SP 6) are elected as the acupuncture points,the electrode pads with wire are attached to the corresponding acupoints, which are connected with Hwato electric acupuncture treatment instrument,TEAS stimulation uses a dense-dispersed wave with frequencies of 2 and 100 Hz alternating every 3 s, and the intensity 5 ~ 12mA,on the first and second days after surgery, the doctor who is responsible for acupuncture will arrive at the ward in the morning and afternoon to administer TEAS stimulation at the same acupoints for 30 min in the TEAS groups
|
|
EXPERIMENTAL: T2 treatment group
TEAS initiates immediately after skin incision and lasts for 30 minutes
|
Basing on the theory of traditional Chinese medicine, bilateral Zusanli (ST 36), Shangjuxu (ST 37) and Sanyinjiao (SP 6) are elected as the acupuncture points,the electrode pads with wire are attached to the corresponding acupoints, which are connected with Hwato electric acupuncture treatment instrument,TEAS stimulation uses a dense-dispersed wave with frequencies of 2 and 100 Hz alternating every 3 s, and the intensity 5 ~ 12mA,on the first and second days after surgery, the doctor who is responsible for acupuncture will arrive at the ward in the morning and afternoon to administer TEAS stimulation at the same acupoints for 30 min in the TEAS groups
|
|
EXPERIMENTAL: T3 treatment group
TEAS initiates immediately after extubating and lasts for 30 minutes
|
Basing on the theory of traditional Chinese medicine, bilateral Zusanli (ST 36), Shangjuxu (ST 37) and Sanyinjiao (SP 6) are elected as the acupuncture points,the electrode pads with wire are attached to the corresponding acupoints, which are connected with Hwato electric acupuncture treatment instrument,TEAS stimulation uses a dense-dispersed wave with frequencies of 2 and 100 Hz alternating every 3 s, and the intensity 5 ~ 12mA,on the first and second days after surgery, the doctor who is responsible for acupuncture will arrive at the ward in the morning and afternoon to administer TEAS stimulation at the same acupoints for 30 min in the TEAS groups
|
|
NO_INTERVENTION: control group
Electrodes are placed on the same acupoints, but no current is given
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the time to first bowel sound
Time Frame: until the time point at which the regular bowel sounds are first heard after surgery up to 1 day
|
It was heard by the same researcher , and defined as the first time point at which the regular bowel sounds (more than two sounds every minute) are first heard after surgery.
|
until the time point at which the regular bowel sounds are first heard after surgery up to 1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the time to first passage of flatus
Time Frame: an average of 24 hours,from the end of surgery to the time of the patient's first passage of flatus
|
This information was obtained with the help of nurse staff and caregivers through questionnaires which were filled out once daily.
|
an average of 24 hours,from the end of surgery to the time of the patient's first passage of flatus
|
|
the time to first passage of defecation
Time Frame: an average of 24 hours,from the end of surgery to the the time of the patient's first passage of defecation,
|
This information was obtained with the help of nurse staff and caregivers through questionnaires which were filled out once daily.
|
an average of 24 hours,from the end of surgery to the the time of the patient's first passage of defecation,
|
|
the first time to normal diet intake
Time Frame: within 48 hours after surgery,from the end of surgery to the time when the patient was given normal diet
|
It was defined as the time at which the patient was given normal diet after defecation without nausea or vomiting
|
within 48 hours after surgery,from the end of surgery to the time when the patient was given normal diet
|
|
the first time to mobilization
Time Frame: within 48 hours after surgery,from the end of surgery to the time when the patient is first able to leave bed
|
It was defined as the time at which the patient is first able to leave bed
|
within 48 hours after surgery,from the end of surgery to the time when the patient is first able to leave bed
|
|
gastroenterological hormones
Time Frame: three time points: before induction of anesthesia, the end of the surgery and the first day after the operation
|
To observe changes in serum levels of gastroenterological hormones ,including serotonin (5-HT), vasoactive intestinal peptide (VIP) and Substance P (SP),venous blood(4ml) will be collected from patients
|
three time points: before induction of anesthesia, the end of the surgery and the first day after the operation
|
|
inflammatory factors
Time Frame: three time points: before induction of anesthesia, the end of the surgery and the first day after the operation
|
To observe changes in serum levels of inflammatory factors,which contain tumor necrosis factor (TNF)-α and interleukin-10 (IL-10),venous blood(4ml) will be collected from patients
|
three time points: before induction of anesthesia, the end of the surgery and the first day after the operation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Fang Li Yang, Xi 'an children's hospital
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 (ANTICIPATED)
June 30, 2022
Primary Completion (ANTICIPATED)
December 30, 2022
Study Completion (ANTICIPATED)
April 30, 2023
Study Registration Dates
First Submitted
May 4, 2022
First Submitted That Met QC Criteria
May 17, 2022
First Posted (ACTUAL)
May 18, 2022
Study Record Updates
Last Update Posted (ACTUAL)
May 18, 2022
Last Update Submitted That Met QC Criteria
May 17, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 2021-015-01
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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