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Application of Cheek Acupuncture Therapy in Patients with Traumatic Multiple Rib Fractures

Application of Cheek Acupuncture Therapy in Patients with Traumatic Multiple Rib Fractures

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123506
Enrollment
Unknown
Registered
2026-04-27
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Multiple Rib Fractures

Interventions

Cheek Acupuncture Group , Control Group:In the Cheek Acupuncture Group, needle insertion was performed at the acupoints before anesthesia induction, and at 24 and 48 hours postoperatively.
Control Group:outine anesthesia protocol with no additional intervention

Sponsors

Beijing Jishuitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 and 65 years. 2.Diagnosed with traumatic multiple rib fractures (=3 ribs confirmed by imaging). 3.Scheduled for open reduction and internal fixation (ORIF) of rib fractures due to meeting surgical indications (e.g., flail chest, severe fracture displacement, respiratory dysfunction, or severe pain). 4.Conscious and able to understand the study protocol and sign the informed consent form. 5.No severe traumatic brain injury or facial trauma. 6.No severe abdominal organ injury or other life-threatening concomitant injuries (e.g., spinal fractures, pelvic fractures, diaphragmatic hernia).

Exclusion criteria

Exclusion criteria: 1.Concomitant severe cardiac, pulmonary, hepatic, or renal insufficiency. 2.History of chronic pain or long-term use of opioids. 3.Facial trauma, infection, deformity, or skin diseases affecting the cheek acupuncture operation area. 4.History of psychiatric disorders or cognitive dysfunction preventing cooperation with the assessment. 5.Pregnant women. 6.Previous history of cheek acupuncture treatment or severe acupuncture phobia (trypanophobia)

Design outcomes

Primary

MeasureTime frame
NRS pain scores at rest and during movement at 24 hours postoperatively;

Secondary

MeasureTime frame
NRS pain scores at rest and during movement at 48 hours postoperatively;Intraoperative remifentanil consumption;Time to first ambulation or time to spontaneous cough;HADS anxiety scores at admission and discharge;

Countries

China

Contacts

Public ContactHao Li

Beijing Jishuitan Hospital, Capital Medical University

lihaowzj@sina.com+86 10 5851 6688

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026