Auricular Pressure for Postoperative Pain After Hemorrhoidectiomy: a Randomized Controlled Trial
Primary Purpose
Postoperative Pain
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Auricular pressure
Shame auricular pressure
Sponsored by
About this trial
This is an interventional treatment trial for Postoperative Pain focused on measuring hemorrhoidectiomy, postoperative pain, auricular pressure
Eligibility Criteria
Inclusion Criteria:
- Meet the diagnostic criteria of grade II-IV mixed hemorrhoids and meet the operation conditions;
- Age 18~65;
- External stripping and internal ligation of mixed hemorrhoids, general anesthesia or lumbar shu point anesthesia;
- VAS score ≥3 points after the implementation of analgesia pump;
- Improve clinical auxiliary examination and sign informed consent.
Exclusion Criteria:
- Combined with inflammatory hemorrhoids, thrombotic hemorrhoids, perianal eczema, perianal abscess and other perianal diseases that affect the evaluation of curative effect;
- Combined with intestinal infectious diseases, intestinal polyps, rectal malignant tumors, etc;
- Combined with severe cardiovascular disease, immune deficiency, mental disorder, or severe liver and kidney dysfunction;
- Auricle skin lesions or auricle skin allergy to tape is difficult to tolerate treatment;
- Combined cognitive impairment could not complete the efficacy; evaluation;
- Pregnancy or planned pregnancy.
Sites / Locations
- Chengdu University of Traditional Chinese Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Auricular pressure
Sham auricular pressure
Arm Description
Use wangbuliuxing seed to stimulate auricular acupuncture point.
Use wangbuliuxing seed to stimulate auricular acupuncture point.
Outcomes
Primary Outcome Measures
Visual Analogue Scale(VAS)
It is a unidimensional measure providing a simple solution for measuring subjective experience. The VAS scale is a 10-cm line with 0 cm indicating no symptoms and 10 cm indicates the greatest extent of symptoms. Twenty-four hours after the operation, VAS>3 in the case of an analgesic pump can be included in the randomized control group.
Secondary Outcome Measures
Hospital Anxiety and Depression scale(HAD)
The HAD scale included measures of anxiety and depression, with scores ranging from 0 to 21. 0-7 points means asymptomatic;A score of 8-10 means suspicious;A score of 11 to 21 means definitely symptomatic( anxiety or depression).
The utilization rate of analgesic drugs(Diclofenac Sodium Dual Release Enteric-coated Capsules)
The ratio of patients using analgesic drugs in each group was calculated (Patients who take bisphenolics once are considered users), and the utilization rate = number of users/total number of users ×100%.
Amount of analgesic drugs (Diclofenac Sodium Dual Release Enteric-coated Capsules)
The total analgesic drugs dose of each group was was considered as the amount of analgesics in the group.
Full Information
NCT ID
NCT04111081
First Posted
September 17, 2019
Last Updated
February 15, 2020
Sponsor
Chengdu University of Traditional Chinese Medicine
1. Study Identification
Unique Protocol Identification Number
NCT04111081
Brief Title
Auricular Pressure for Postoperative Pain After Hemorrhoidectiomy: a Randomized Controlled Trial
Official Title
Pilot Study of Clinical Randomized Controlled Trial of Auricular Pressure Therapy for Intervention of Postoperative Pain of Hemorrhoidectiomy
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2020 (Anticipated)
Primary Completion Date
July 1, 2021 (Anticipated)
Study Completion Date
July 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chengdu University of Traditional Chinese Medicine
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Auricular pressure is effective for postoperative analgesia after hemorrhoidectomy, but the evidence is not sufficient.
Detailed Description
This is a randomized, double-blind study to study the analgesic effect of auricular pressure pill on persistent pain after hemorrhoidectiomy. Baseline pain intensity scores (VAS>3) of the subjects will be collected 24 hours after the operation of the patients. Eligible subjects will be randomly assigned to receive auricular pressure pills or sham-auricular pressure pills. The treatment will last 5-7 days. Participants will receive auricular pressure once two days, and receive VAS, concomitant medication, PONV intensity scale and peripheral edema were recorded daily, and after the operation 24 hours, 3 days and 7 days the patients will receive anxiety and depression scale(HAD) , and VAS data will be collected by telephone at 3 and 6 months after the operation.
The statistical analysis results will be subject to the full analysis set (FAS) results, and a sensitivity analysis will be performed comparing the per-protocol (PP). The main indicators will be analyzed by covariance analysis, with VAS results as the dependent variable, grouping as the random factor, and age, course of disease, surgical method and baseline as the covariables to correct the P value. The secondary indicator analgesic usage rate will be analyzed using logistic regression analysis. Whether analgesic will be used as a dependent variable, grouping as a random factor, and age, course of disease, surgical method and evaluation time point will be analyzed as covariables. Other outcome indicators will be analyzed by covariance analysis, and the model will be the same as that of the main indicators. P<0.05 considered as significant difference, and SPSS20.0 used for analysis.
The purpose of this study was to seek high quality evidence-based medical evidence for intervention of auricular pressure pills on postoperative pain of hemorrhoidectomy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Pain
Keywords
hemorrhoidectiomy, postoperative pain, auricular pressure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Auricular pressure
Arm Type
Experimental
Arm Description
Use wangbuliuxing seed to stimulate auricular acupuncture point.
Arm Title
Sham auricular pressure
Arm Type
Sham Comparator
Arm Description
Use wangbuliuxing seed to stimulate auricular acupuncture point.
Intervention Type
Other
Intervention Name(s)
Auricular pressure
Intervention Description
Select related auricular points: Shenmen(TF4), sympathetic(AH6a), rectum(HX2), anus(HX5), stomach(CO4), subcortical(AT4). The auricle skin of the patient was disinfected 24 hours after the operation, and wanghuoxing seed will be used for stimulation. Ask patients press every two hours for one minute at each point. When the pain is severe, do pressure compressions at each point for 2 minutes once hour.
Intervention Type
Other
Intervention Name(s)
Shame auricular pressure
Intervention Description
Select unrelated auricular points: eye(LO5), occipital(AT3), tonsil(LO7,8,9), lower auricular root(R3), dorsum auricular kidney(P5) and dorsum auricular lung(P2). The auricle skin of the patient was disinfected 24 hours after the operation, and wanghuoxing seed will be used for stimulation. Ask patients press every two hours for one minute at each point. When the pain is severe, do pressure compressions at each point for 2 minutes once hour.
Primary Outcome Measure Information:
Title
Visual Analogue Scale(VAS)
Description
It is a unidimensional measure providing a simple solution for measuring subjective experience. The VAS scale is a 10-cm line with 0 cm indicating no symptoms and 10 cm indicates the greatest extent of symptoms. Twenty-four hours after the operation, VAS>3 in the case of an analgesic pump can be included in the randomized control group.
Time Frame
Day 1 after randomization.
Secondary Outcome Measure Information:
Title
Hospital Anxiety and Depression scale(HAD)
Description
The HAD scale included measures of anxiety and depression, with scores ranging from 0 to 21. 0-7 points means asymptomatic;A score of 8-10 means suspicious;A score of 11 to 21 means definitely symptomatic( anxiety or depression).
Time Frame
Twenty-four hours, three days, and seven days after surgery
Title
The utilization rate of analgesic drugs(Diclofenac Sodium Dual Release Enteric-coated Capsules)
Description
The ratio of patients using analgesic drugs in each group was calculated (Patients who take bisphenolics once are considered users), and the utilization rate = number of users/total number of users ×100%.
Time Frame
Day 7 after randomization.
Title
Amount of analgesic drugs (Diclofenac Sodium Dual Release Enteric-coated Capsules)
Description
The total analgesic drugs dose of each group was was considered as the amount of analgesics in the group.
Time Frame
Day 7 after randomization.
Other Pre-specified Outcome Measures:
Title
Tissue edema
Description
The degree of tissue edema was observed and recorded truthfully.
Time Frame
Day 3, day4, day5, day6 and day7 after randomization.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Meet the diagnostic criteria of grade II-IV mixed hemorrhoids and meet the operation conditions;
Age 18~65;
External stripping and internal ligation of mixed hemorrhoids, general anesthesia or lumbar shu point anesthesia;
VAS score ≥3 points after the implementation of analgesia pump;
Improve clinical auxiliary examination and sign informed consent.
Exclusion Criteria:
Combined with inflammatory hemorrhoids, thrombotic hemorrhoids, perianal eczema, perianal abscess and other perianal diseases that affect the evaluation of curative effect;
Combined with intestinal infectious diseases, intestinal polyps, rectal malignant tumors, etc;
Combined with severe cardiovascular disease, immune deficiency, mental disorder, or severe liver and kidney dysfunction;
Auricle skin lesions or auricle skin allergy to tape is difficult to tolerate treatment;
Combined cognitive impairment could not complete the efficacy; evaluation;
Pregnancy or planned pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hui Zheng, PhD
Organizational Affiliation
Chengdu University of Traditional Chinese Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chengdu University of Traditional Chinese Medicine
City
Chengdu
State/Province
Sichuan
ZIP/Postal Code
610075
Country
China
12. IPD Sharing Statement
Learn more about this trial
Auricular Pressure for Postoperative Pain After Hemorrhoidectiomy: a Randomized Controlled Trial
We'll reach out to this number within 24 hrs