Trial · NCT07895329
Shiwei Anshen Granules for Chronic Insomnia
NCT07895329, Not applicable, Not yet recruiting, Dongzhimen Hospital, Beijing
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Shiwei Anshen Granules for Chronic Insomnia. Trials, record NCT07895329. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07895329
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Shiwei Anshen Granules for Chronic Insomnia
- NCT number
- NCT07895329
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 240 participants, estimated
- Lead sponsor
- Dongzhimen Hospital, Beijing
- Conditions
- Chronic Insomnia
- Interventions
- Shiwei Anshen granules, Placebo granules
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Pittsburgh Sleep Quality Index (PSQI) total score | Baseline, 4 weeks, 8 weeks after treatment | The change of PSQI total score from baseline to week 8. Lower score indicates better sleep quality. |
| Secondary | Insomnia Severity Index (ISI) score change | Baseline, 4 weeks, 8 weeks | Change of ISI score from baseline to week 8 to assess insomnia severity |
| Secondary | Traditional Chinese Medicine Syndrome Score change | Baseline, 4 weeks, 8 weeks | Variation of TCM syndrome score before and after intervention |
| Secondary | Adverse events | Baseline, 4 weeks, 8 weeks | Incidence of adverse events during the 8-week treatment period to evaluate safety. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 40904305 | RESULT |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07895329
GET https://conductscience.org/api/trials/v1/NCT07895329/registered