The clinical observation of Zhang's experience prescription combined with ear point for pain after hand trauma of qi stagnation and blood stasis

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300076909

Enrollment

Unknown

Registered

2023-10-24

Start date

2023-10-30

Completion date

Unknown

Last updated

2023-10-30

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

Conditions

Pain after hand trauma

Interventions

zhangshi group:On the basis of the control group, the directed transdrug therapy with Zhang's empirical prescription was implemented

auricular point group:On the basis of the control group, the ear point acupuncture treatment was performed

unite group:On the basis of the control group, Zhang's experience prescription combined with ear point acupuncture was performed

contrast group:Conventional treatment and nursing care for postoperative pain in patients with hand trauma. The patients woke up after anesthesia and had NRS score > 3 for the first time were given re

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria for hand trauma and are hospitalized after surgery; (2) The postoperative TCM syndrome type was Qi-stagnation and blood-stasis type (3) Postoperative pain score (NRS) > 3; (4) Age =18 years old, gender is not limited; (5) Patients without mental illness, cognitive impairment and consciousness disorder, who can cooperate with treatment after surgery; (6) Informed and willing to participate in the study.

Exclusion criteria

Exclusion criteria: (1) Those who are participating in other clinical trials; (2) Patients using intravenous analgesia pump after surgery; (3) Patients with multiple fractures or compound injuries; (4) Patients who are allergic to Chinese herbal medicine or have skin diseases such as contact dermatitis; (5) Skin damage at selected acupoints; (6) Patients with cardiac pacemakers; (7) Women during pregnancy; (8) Patients with serious medical diseases that affect the progress of this study. (6) Informed and willing to participate in the study.

Design outcomes

Primary

Measure	Time frame
NRS;	—

Secondary

Measure	Time frame
clinical effects;Peripheral blood circulation;adverse reaction;72-hour remedial analgesia rate;	—

Countries

China

Contacts

Public ContactQinqin Li

Hangzhou Fuyang Traditional Chinese medicine bone injury hospital

552302525@qq.com+86 151 5819 0345

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026