Insomnia Clinical Trial
Official title:
Clinical Study of Auricular Point Seed Burying Combined With Fire Dragon Pot Moxibustion in Perimenopausal Women With Insomnia
Verified date | February 2022 |
Source | Anhui Medical University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Insomnia in perimenopausal women is normal. Studies have shown that insomnia occurs in 75-81% of perimenopausal women and is 2.4 times more common than in premenopausal participants. Western medicine often uses sedative sleeping drugs in the treatment of insomnia in perimenopausal women, which have better effects but have more side effects, and whether they are suitable for long-term application is still controversial. Non-pharmacological traditional therapies in Traditional Chinese Medicine have achieved significant clinical efficacy in the treatment of perimenopausal insomnia patients in recent years. This study aims to explore the efficacy of auricular point seed burying combined with fire dragon pot moxibustion in the treatment of the insomnia symptoms of perimenopausal women.
Status | Completed |
Enrollment | 70 |
Est. completion date | October 30, 2020 |
Est. primary completion date | October 30, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - All participants met the diagnosis of perimenopausal insomnia as described in the Chinese Guidelines for the Diagnosis and Treatment of Adult Insomnia (2017 Edition). - Pittsburgh Sleep Quality Index (PSQI) >7. - Insomnia at least 3 times per week and lasting for more than 1 month. - Onset around menopause with menstrual disorders. - No contraindications to auricular seed burial and fire dragon pot moxibustion treatment - Informed consent. Exclusion Criteria: - Those with a duration of less than 1 week or those who have received other relevant treatment within the last month that affects the observation of efficacy - Secondary insomnia due to physical illness or psychological disorders. - Participants with severe co-morbidities and psychiatric disorders. - Those who refuse to cooperate with treatment. - Those who use other methods of treatment during the treatment period, which affects the judgment of efficacy. |
Country | Name | City | State |
---|---|---|---|
China | The Third Affiliated Hospital of Anhui Medical University (The first people ' s Hospital of Hefei) | Hefei | Anhui |
Lead Sponsor | Collaborator |
---|---|
Weihua Yu |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The score of Pittsburgh Sleepiness Quantifier Inventory | The score of Pittsburgh Sleepiness Quantifier Inventory (PSQI) was compared between the two groups of patients before and after the intervention (For details, please refer to the literature: The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research). A PSQI score <7 is considered good sleep quantity and =7 is poor sleep quality, and the higher the patient score, the worse the sleep quality. | one month | |
Secondary | Adverse reactions | Observe whether erythema, blisters, allergic and other adverse reactions are appearing | one month |
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