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Treatment of Chronic Insomnia According to Yin Yang Theory and Its Correlation With Circadian Rhythm

Primary Purpose

Chronic Insomnia, Circadian Rhythm, Traditional Chinese Medicine

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Suanzaoren Decoction and Huanglian Wendan Decoction
Estazolam 1Mg Tab
Sponsored by
The First Affiliated Hospital with Nanjing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Insomnia

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Outpatients or inpatients.
  • It conforms to the chronic insomnia diagnosis standard of Chinese adult insomnia diagnosis and treatment guide (2017 Edition).
  • Chronic insomnia patients with Yin yang imbalance and Ying Wei Disharmony Syndrome.
  • Informed consent, voluntary participation in the study.

Exclusion Criteria:

  • Sleep apnea syndrome leads to insomnia.
  • Severe depression, suicidal tendency or having committed suicide.
  • Pregnant and lactating women.
  • It has serious primary heart, liver, lung, kidney, blood or serious diseases affecting its survival, such as: tumor or AIDS, SCR > 1.5n (n is the upper limit of normal value), ALT > 2n (n is the upper limit of normal value), WBC < 3.0 × 109 / L;
  • Those who cannot give full informed consent due to mental disorders.
  • According to the researcher's judgment, other situations that are not suitable for the group, such as the change of working environment.
  • Subjects who are participating in other clinical studies.

Sites / Locations

  • The First Affiliated Hospital of Nanjing Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Chinese medicine group

Western medicine group

Arm Description

Participants received Suanzaoren Decoction and Huanglian Wendan Decoction orally twice daily for 4 weeks. Subjects who had previously taken Western medicine hypnotics continued to take them, and those who did not take them did not add Western medicine hypnotics.

Participants received Estazolam 1mg tablet orally once daily for 4 weeks.

Outcomes

Primary Outcome Measures

Change from Baseline in the total score of the Pittsburgh sleep quality index (PSQI) at 4 weeks
The Pittsburgh sleep quality index (PSQI) is a validated,self-reported instrument assessing the sleep quality over the past 4 week period. Possible scores range from 0(the best sleep quality) to 21(the worst possible sleep) quality).The higher the score of PSQI, the worse the sleep quality. Change=(Month 1 Score-Baseline Score)
Cessation rate of Western medicine hypnotics at Month 6
Cessation was defined as an absence of any Western medicine hypnotics that was sustained for 3 consecutive months or more. Cessation rate of Western medicine hypnotics=(Month 6 number-Baseline number)/Baseline number of Participants use Western medicine hypnotics.

Secondary Outcome Measures

Change from Baseline of the ALT at 4 weeks
Alanine aminotransferase, ALT in U/L
Change from Baseline of the AST at 4 weeks
Aspartate aminotransferase, AST in U/L
Change from Baseline of the BUN at 4 weeks
Blood urea nitrogen, BUN in mmol/L
Change from Baseline of the Scr at 4 weeks
Serum creatinine, Scr in μmol/L
Genome-wide association study
Illumina HumanHap550-Duo BeadChips was used to perform the whole genome genotyping in deCODE genetics(Reykjavı'k, Iceland)
Change from Baseline in the score of Morningness-Eveningness Questionaire (MEQ)
The MEQ is a validated, self-reported questionaire assessing personal chronotype in the recent period. Possible scores range from 16 (extreme eveningness) to 86 (extreme morningness). Change = (Week 4 Score - Baseline Score). Positive score change indicates a shift from eveningness to morningness.
Change from baseline objective sleep quality
Objective sleep quality data is assessed by wearing a Sleep wearable devices

Full Information

First Posted
July 6, 2022
Last Updated
February 15, 2023
Sponsor
The First Affiliated Hospital with Nanjing Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT05452577
Brief Title
Treatment of Chronic Insomnia According to Yin Yang Theory and Its Correlation With Circadian Rhythm
Official Title
Clinical Normative Evaluation of Chronic Insomnia Treated by Traditional Chinese Medicine According to Yin Yang Theory and Its Correlation With Circadian Rhythm
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 22, 2021 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First Affiliated Hospital with Nanjing Medical University

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
The purpose of this study is to assess the safety and efficacy of Traditional Chinese medicine (TCM) according to Yin Yang theory for treatment of chronic insomnia .
Detailed Description
All subjects giving written informed consent. In this multicenter, controlled, prospective cohort study, the outpatient and inpatient chronic insomnia patients' baseline demographic data were collected, including age, gender, education background, and medication history. Venous blood samples were collected and sent to laboratory test for blood routine, and blood biochemistry at Baseline and Week 4. The Pittsburgh sleep quality index (PSQI) was used to assess the patients' sleep quality at baseline and week 4. Objective sleep quality data is assessed by wearing a Sleep wearable devices. The classic Morningness-Eveningness Questionnaire and wearable devices was used to assess the patients' chronotype at baseline and week 4.Subjects who visit the TCM clinic of this project received Suanzaoren Decoction and Huanglian Wendan Decoction orally twice daily for 4 weeks. Add or subtract Chinese herbal medicine according to the different clinical manifestations of each patient. Subjects from TCM clinic who had previously taken Western medicine hypnotics continued taking them, and for those who had not taken before, Western medicine hypnotics shall not be given/prescribed. Subjects who visit the Western medicine clinic of this project received Estazolam 1mg tablet orally once daily for 4 weeks. The participants will have a follow-up visit every two weeks, and the prescription would be adjusted according to the condition of illness.Cessation rate of Western medicine hypnotics was assessed at Month 6.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Insomnia, Circadian Rhythm, Traditional Chinese Medicine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
186 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Chinese medicine group
Arm Type
Experimental
Arm Description
Participants received Suanzaoren Decoction and Huanglian Wendan Decoction orally twice daily for 4 weeks. Subjects who had previously taken Western medicine hypnotics continued to take them, and those who did not take them did not add Western medicine hypnotics.
Arm Title
Western medicine group
Arm Type
Active Comparator
Arm Description
Participants received Estazolam 1mg tablet orally once daily for 4 weeks.
Intervention Type
Drug
Intervention Name(s)
Suanzaoren Decoction and Huanglian Wendan Decoction
Other Intervention Name(s)
Wild Jujube Seed Decoction and Huanglian Wendan Decoction
Intervention Description
Twice daily. Chinese herbal medicine includes: includes: 25 grams of Suanzaoren, 10 grams of chuanxiong, 30 grams of fushen, 10 grams of Polygala tenuifolia, 10 grams of Pinellia ternata, 12 grams of tangerine peel, 15 grams of Zhuru, 30 grams of forged keel, 30 grams of forged oyster,10 grams of aurantii fructus, 6 grams of coptis chinensis, 30 grams of Albizzia bark.Add or subtract Chinese herbal medicine according to the different clinical manifestations of each patient.
Intervention Type
Drug
Intervention Name(s)
Estazolam 1Mg Tab
Other Intervention Name(s)
Estazolam, Estazolam Tablets, Estazolam Pill
Intervention Description
1mg tablet once daily
Primary Outcome Measure Information:
Title
Change from Baseline in the total score of the Pittsburgh sleep quality index (PSQI) at 4 weeks
Description
The Pittsburgh sleep quality index (PSQI) is a validated,self-reported instrument assessing the sleep quality over the past 4 week period. Possible scores range from 0(the best sleep quality) to 21(the worst possible sleep) quality).The higher the score of PSQI, the worse the sleep quality. Change=(Month 1 Score-Baseline Score)
Time Frame
Baseline and Week 4
Title
Cessation rate of Western medicine hypnotics at Month 6
Description
Cessation was defined as an absence of any Western medicine hypnotics that was sustained for 3 consecutive months or more. Cessation rate of Western medicine hypnotics=(Month 6 number-Baseline number)/Baseline number of Participants use Western medicine hypnotics.
Time Frame
Month 6
Secondary Outcome Measure Information:
Title
Change from Baseline of the ALT at 4 weeks
Description
Alanine aminotransferase, ALT in U/L
Time Frame
Baseline and Week 4
Title
Change from Baseline of the AST at 4 weeks
Description
Aspartate aminotransferase, AST in U/L
Time Frame
Baseline and Week 4
Title
Change from Baseline of the BUN at 4 weeks
Description
Blood urea nitrogen, BUN in mmol/L
Time Frame
Baseline and Week 4
Title
Change from Baseline of the Scr at 4 weeks
Description
Serum creatinine, Scr in μmol/L
Time Frame
Baseline and Week 4
Title
Genome-wide association study
Description
Illumina HumanHap550-Duo BeadChips was used to perform the whole genome genotyping in deCODE genetics(Reykjavı'k, Iceland)
Time Frame
Month 6
Title
Change from Baseline in the score of Morningness-Eveningness Questionaire (MEQ)
Description
The MEQ is a validated, self-reported questionaire assessing personal chronotype in the recent period. Possible scores range from 16 (extreme eveningness) to 86 (extreme morningness). Change = (Week 4 Score - Baseline Score). Positive score change indicates a shift from eveningness to morningness.
Time Frame
Baseline and Week 4
Title
Change from baseline objective sleep quality
Description
Objective sleep quality data is assessed by wearing a Sleep wearable devices
Time Frame
Baseline and Week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Outpatients or inpatients. It conforms to the chronic insomnia diagnosis standard of Chinese adult insomnia diagnosis and treatment guide (2017 Edition). Chronic insomnia patients with Yin yang imbalance and Ying Wei Disharmony Syndrome. Informed consent, voluntary participation in the study. Exclusion Criteria: Sleep apnea syndrome leads to insomnia. Severe depression, suicidal tendency or having committed suicide. Pregnant and lactating women. It has serious primary heart, liver, lung, kidney, blood or serious diseases affecting its survival, such as: tumor or AIDS, SCR > 1.5n (n is the upper limit of normal value), ALT > 2n (n is the upper limit of normal value), WBC < 3.0 × 109 / L; Those who cannot give full informed consent due to mental disorders. According to the researcher's judgment, other situations that are not suitable for the group, such as the change of working environment. Subjects who are participating in other clinical studies.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiuqin Wang, doctor
Phone
+86-25-68306156
Email
xiuqinw@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiuqin Wang, doctor
Organizational Affiliation
The First Affiliated Hospital with Nanjing Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The First Affiliated Hospital of Nanjing Medical University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
224000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiuqin Wang, doctor
Phone
+86-25-68306156
Email
xinqinw@126.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Treatment of Chronic Insomnia According to Yin Yang Theory and Its Correlation With Circadian Rhythm

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