Evaluation of Clinical Effect of Acupuncture on Acute Exacerbation of Bronchial Asthma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHenan University of Traditional Chinese Medicine

About this trial

Based on the bioholographic theory, this study preliminarily explores the clinical efficacy of hand acupuncture in treating acute exacerbation of bronchial asthma and evaluates its immediate anti-asthmatic effect, so as to provide a new therapeutic strategy for the clinical management of bronchial asthma.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients meeting the Western medicine diagnostic criteria for acute exacerbation of bronchial asthma

Aged ≥ 18 years old

Voluntarily receive treatment and sign the informed consent form

Disqualifiers

Those who fail to meet the inclusion criteria

Patients suffering from other severe systemic diseases such as diseases of the circulatory system, hematological system and nervous system

Pregnant or lactating women

Subjects enrolled but not treated per the study protocol

Trial design

Design model

Parallel

Treatments tested in this trial

  • Acupuncture

    Other intervention

    The acupoints selected were Kechuan point, New Kechuan point, and Yuji point. The treatment was administered once a day for 20 minutes each time, for 5 consecutive days.

  • Standard Western medicine treatment

    Drug

    Evaluate and manage in accordance with the Chinese Expert Consensus on Assessment and Management of Acute Exacerbation of Bronchial Asthma issued by the Asthma Group of the Chinese Thoracic Society, Chinese Medical Association in 2018 and the Guidelines for the Prevention and Treatment of Bronchial Asthma (2020 ).

Treatment groups

72 Participants
are divided into 2 treatment groups
Group A: acupuncture groupExperimental treatment 2 interventions
Group B: control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Peak Expiratory Flow(PEF)

PEF will be used to assess pulmonary function

Time frame
After treatment on Day 5 and follow-up at 1, 2 and 3 months
2

Asthma Control Test

The ACT score consists of 5 questions, each scored from 1 to 5 points, with a total score ranging from 5 to 25 points; lower scores indicate more severe symptoms.

Time frame
After treatment on Day 5 and follow-up at 1, 2 and 3 months

Secondary outcomes

1

Forced expiratory volume in first second/pred(FEV1%pred)

FEV1%pred will be used to assess pulmonary function

Time frame
After treatment on Day 5 and follow-up at 1, 2 and 3 months
2

Clinical Symptom and Sign Score

It includes six symptoms: cough, expectoration, chest tightness, wheezing, shortness of breath and wheeze. Scores of 0, 3, 6 and 9 are assigned according to the severity of symptoms, with higher scores corresponding to more severe symptoms.

Time frame
After treatment on Day 5 and follow-up at 1, 2 and 3 months
3

Mini Asthma Quality of Life Questionnaire(Mini-AQLQ)

It consists of 15 questions, each scored on a scale from 1 to 7 based on the severity of symptoms and their degree of impact. A score of 1 indicates no symptoms or no adverse impacts, while a score of 7 stands for severe symptoms or substantial impairment. Lower total scores correspond to a higher quality of life.

Time frame
After treatment on Day 5 and follow-up at 1, 2 and 3 months
4

modified Medical Research Council (mMRC)

Scores range from 0 to 4 based on the severity of dyspnea, with higher scores indicating more severe symptoms.

Time frame
After treatment on Day 5 and follow-up at 1, 2 and 3 months

Other outcomes

Sponsors and contacts

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