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Modified Tian Wang Bu Xin Dan Hydrogel Patch in Preventing Postoperative Delirium in Elderly Patients

Modified Tian Wang Bu Xin Dan Hydrogel Patch in Preventing Postoperative Delirium in Elderly Patients: A Muticenter Randomised Control Trial

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04947761
Enrollment
200
Registered
2021-07-01
Start date
2021-07-13
Completion date
2022-12-31
Last updated
2021-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Delirium

Brief summary

The purpose of this study is to determine whether preoperative administration of Modified Tian Wang Bu Xin Dan Hydrogel Patch prevents the incidence of postoperative delirium in elderly patients undergoing major surgery.

Detailed description

The Traditional Chinese Medicine (TCM) Tian Wang Bu Xin Dan (TWBXD, Cheonwangbosimdan), first recorded in Effective Formulae Handed Down for Generations ( Shi Yi De Xiao Fang) in 1337, is a herbal medicine that has been continuously utilized in Chinese medicine. It alleviates insomnia, anxiety, and palpitation by furnishing energy and stabilizing patients' mind. Cheonwangbosimdan can mitigate primary insomnia and secondary insomnia in patients with hyperthyroidism and menopause without severe side effects. Tianwang Buxin Decoction has the same effect as Olanzapine for the treatment of delirium after hip joint replacement in falling-induced senile femoral neck fracture patients. This study aim to evaluate the incidence of postoperative delirium in elderly patients treated with prophylactic Modified Cheonwangbosimdan Hydrogel Patch versus placebo patch.

Interventions

DRUGmodified Tian Wang Bu Xin Dan hydrogel patch

modified Cheonwangbosimdan hydrogel patch (one patch/24 hours) applied to Shenque point for 4 days (1 patch daily beginning 2 days preoperative, and continued at 1 patch daily until 2 days postoperatively)

OTHERplacebo patch

placebo patch (one patch/24 hours) applied to Shenque point for 4 days (1 patch daily beginning 2 days preoperative, and continued at 1 patch daily until 2 days postoperatively)

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients' age ≥70 years; 2. Underwent elective non-cardiac surgery (including Orthopedics, thoracic, urology, general surgery patients)under general anesthesia ;

Exclusion criteria

1. History of neuropsychiatric diseases including delirium, mental disorders, Parkinson, dementia, etc.; 2. The operation was cancelled due to various reasons after the patient was enrolled; 3. severe liver disease; severe renal dysfunction defined as either having creatinine clearance \< 30 ml/min or being dialysis-dependent; 4. Patients who undergo second operation in a short period; 5. Past 30-day prescribed use of sedative-hypnotics for the indication of insomnia; 6. History of alcohol abuse or a history of drug dependence; 7. Cannot with the completion of tests of cognitive function; 8. Known allergy to skin patch; 9. Treatment site has active skin lesion or inflammation; 10. Refused to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of inpatient post-operative delirium as measured using the 3D-confusion assessment method (3D-CAM)Day 1 postoperativelyOccurrence of delirium on any postoperative day, as assessed using the 3D-CAM or CAM-ICU daily

Secondary

MeasureTime frameDescription
Athens Insomnia ScaleBaseline and 1,2,3 days after surgeryusing the Athens Insomnia Scale to test the subjective sleep quality of patients. The range were from 0-3. Total score \< 4 means sleep well; total score =6 means suspicious of insomnia; total score \> 6 means insomnia.
Pain at rest using Numerical Rating Scale(NRS)postoperative days 1, 2, 3NRS pain scores will also be measured at rest. The NRS is a validated 11-point numerical scale that ranges from 0 (no pain) to 10 (worst pain possible).
Total postoperative analgesic requirementsFirst 48 hours postoperativelyAmount of opioid (IV morphine or hydromorphone) and oral analgesics required for pain control, reported as overall morphine equivalents.
Sleep QualityBaseline and 1,3 days after surgeryObjective sleep quality will be measured using a Fitbit Charge 3 activity monitor to be worn
Change in biological markers (2)Baseline and 1 day after surgeryPlasma levels of S100B
STOP-Bang scoreBaselineSTOP-BANG questionnaire
Pittsburgh Sleep Quality IndexBaseline and day 3 postoperativelyThe PSQI is filled out by the patient and assesses patient sleep quality.
Change in biological markers (1)Baseline and 1 day after surgeryPlasma levels of CXCL13

Countries

China

Contacts

Primary ContactWeidong Mi, PhD
wwdd1962@aliyun.com8613381082966
Backup ContactChunlei Ouyang, PhD
ouyangchunlei@gmail.com+8618810300815

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026