The Promotion Plan of Moxibustion on Ulcerate Colitis

Sponsor
Shanghai Institute of Acupuncture, Moxibustion and Meridian (Other)
Overall Status
Completed
CT.gov ID
NCT03232528
Collaborator
(none)
128
1
2
37.9
3.4

Study Details

Study Description

Brief Summary

To evaluate the efficacy of Moxibustion in the treatment of Ulcerative Colitis, thus the scientific foundation for rational use of Moxibustion in clinical usage, in order to find admission of the Acupuncture and Moxibustion and even medicine field, accomplish popularization and application.

Condition or Disease Intervention/Treatment Phase
  • Other: Herb-partitioned moxibustion
  • Other: Sham herb-partitioned moxibustion
N/A

Detailed Description

A total of 128 patients with UC were randomly divided into the following 2 groups: a) Herb-partition moxibustion (Treatment Group) and b) Sham herb-partition moxibustion (Control Group). All patients in the trial will be treated with moxibustion 3 times a week, once a day for 30 minutes, for a total of 12 weeks. After treating the treatment had ended and the 52nd week of follow-up to observe the clinical therapy effect of Moxibustion in UC patients. Tissue morphology and molecular biology tests will be conducted to observe the regulation in the intestinal mucosa of UC patients. All these steps will be done in order to provide clinical usage for the effects of herb-partition moxibustion in the treatment of UC.

Study Design

Study Type:
Interventional
Actual Enrollment :
128 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
A Study on the Promotion Plan of the Moxibustion Treatment of Ulcerate Colitis
Actual Study Start Date :
Nov 1, 2016
Actual Primary Completion Date :
Dec 30, 2018
Actual Study Completion Date :
Dec 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Herb-partitioned moxibustion

Drug: Herbal cake, Device: Moxibustion. Herbal cakes formula: Monkshood 10g, Cinnamon 2g, Salvia miltiorrhiza 3g, Flos Carthami 3g, Radix Aucklandiae 2g. Herbs are smashed into powder. Every 2.5g medicine powder is mixed with 3g millet wine and then pressed into herbal cakes using a specific mold. Each cake should be 23mm in diameter and 5mm in height. Then, ignited moxa cones are placed on top of each herbal cake. Herbal cakes with moxa cones will be positioned at acupuncture points ST25, ST37 and CV6. The entire treatment will be done once a day for 1 moxa cone every acupuncture point, 30 minutes at a time, 3 times a week, for a total of 12 weeks.

Other: Herb-partitioned moxibustion
Patients receive herb-partition moxibustion 3 times a week, once a day for 30 minutes, for a total of 12 weeks.
Other Names:
  • Treatment Group
  • Sham Comparator: Sham herb-partitioned moxibustion

    Drug: Herbal cake, Device: Sham moxibustion. Herbal cakes formula: Monkshood 10g, Cinnamon 2g, Salvia miltiorrhiza 3g, Flos Carthami 3g, Radix Aucklandiae 2g. Herbs are smashed into powder. Every 2.5g medicine powder is mixed with 3g millet wine and then pressed into herbal cakes using a specific mold. Each cake should be 23mm in diameter and 5mm in height. Then, ignited moxa cones are placed on top of each herbal cake. Small cardboard sheets with the same size as the herbal cakes will be wrapped with aluminum foil and placed under each herbal cake. These herbal cakes will be positioned at acupuncture points ST25, ST37 and CV6. The entire treatment will be done once a day for 1 moxa cone every acupuncture point, 30 minutes at a time, 3 times a week, for a total of 12 weeks.

    Other: Sham herb-partitioned moxibustion
    Patients receive sham herb-partition moxibustion 3 times a week, once a day for 30 minutes, for a total of 12 weeks.
    Other Names:
  • Control Group
  • Outcome Measures

    Primary Outcome Measures

    1. total effective rate [3 months]

      The curative effect of Herb-partitioned moxibustion for 128 UC patients.

    Secondary Outcome Measures

    1. Mayo score [6 months]

      Assay for the ulcerative colitis desease activity index. It is constructed by four scales, Including stool frequency、rectal bleeding、mucosal appearance at endoscopy and physician rating of disease activity. Every scale can be scored with o ,1 ,2 or 3 according to the activity index of scale. Scores should be compared to previous scores taken for a patient. The higher the score (minimum 0 point and maximum 12 points), the more severe the ulcerative colitis.

    2. symptom score [3 months]

      Observe the abdominal pain, bloody stool, intolerance of cold, soreness and weakness of waist an knees, diarrhea, mucous stool, tenesmus, anorexia and lassitude score.

    3. Visual Analogue Scale(VAS) [6 months]

      Observe the degree of abdominal pain

    4. Inflammatory Bowel Disease Questionnaire(IBDQ) [6 months]

      Life quality was determined by the total score of the 32 questions. Each question is given 1-7 different degrees of answer. One represents the heaviest degree and seven represents the lightest degree. The lower the score (minimum 32 points and maximum 224 points), the worse the life quality.

    5. Hospital Anxiety and Depression Scale(HADS) [3 months]

      The HADS is a fourteen item scale that generates ordinal data. Seven of the items relate to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 .The higher the total score (minimum 0 point and maximum 21 points), the more severe the anxiety or depression.

    6. Laboratory tests for disease activity: C-reaction protein [6 months]

      Assay for the quantification of total C-reaction protein in serum.(Normal reference value:<10mg/L)

    7. Laboratory tests for disease activity: Erythrocyte sedimentation rate [6 months]

      Assay for the quantification of total Erythrocyte sedimentation rate in serum.(Normal reference value: male 0~15mm/h; female 0~20mm/h)

    8. gut mucosal score under the endoscopy: Baron score; [3 months]

      evaluate the gut mucosal state by using electronic colonoscopy

    9. mucosal pathology:Geboes score [3 months]

      Observe the intestinal mucosal tissue changes by HE staining

    Other Outcome Measures

    1. Safety Assessment [3 months]

      With Administration Events reports record the adverse reaction treatment process, with the moxibustion treatment of safety evaluation. Such as the incidence and severity of scald, skin allergic, vasodepressor syncope etc. Also record subjects's vital signs, consist of body temperature, blood pressure and pulse.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Meet the diagnosis of UC

    • Patients do not receive any medicine, or if they are receiving medicine, it should be aminosalicylates and/or prednisone (dose ≤15mg and have taken at least 1 month);

    • Patients should have not received antibiotic, biologicals within 3 months prior to entering the study;

    • Signing a written informed consent.

    Exclusion Criteria:
    • Patients with cardiac, encephalic, hepatic, nephric, hematopoietic system, psychotic or any other serious diseases;

    • Pregnancy or lactation;

    • genetic family history of nervous system disease

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Shanghai Research Insititute of Acupuncture and Meridian Shanghai Xuhui China 20000

    Sponsors and Collaborators

    • Shanghai Institute of Acupuncture, Moxibustion and Meridian

    Investigators

    • Study Director: Huangan Wu, Doctor, Shanghai Institute of Acupuncture-Moxibustion and Meridian, Shanghai University of Traditional Chinese Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Shanghai Institute of Acupuncture, Moxibustion and Meridian
    ClinicalTrials.gov Identifier:
    NCT03232528
    Other Study ID Numbers:
    • promotion
    First Posted:
    Jul 28, 2017
    Last Update Posted:
    Mar 18, 2021
    Last Verified:
    Mar 1, 2021
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 18, 2021