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Effect of buccal needle therapy on pain after daytime ankle internal fixation

Effect of buccal needle therapy on pain after daytime ankle internal fixation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092042
Enrollment
Unknown
Registered
2024-11-07
Start date
2024-11-07
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Extraction of internal fixation of ankle joint during the day

Interventions

Cheek needle therapy group (Group A):Cheek needle before general anesthesia
General anesthesia Group (Group C):General anethesia

Sponsors

Lu’an Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) ASA Grade I-II daytime ankle fixation extraction patients (2) Age 18-60. (3) Agree to participate in this study and sign the "informed consent"

Exclusion criteria

Exclusion criteria: (1) The patient has a mental disorder or communication disorder; (2) Patients with serious primary diseases of heart, lung, liver, kidney and hematopoietic system; (3) Allergic to any of the drugs in the study; (4) Abnormal coagulation function; (5) Addiction to toxic narcotic drugs or recent use of non-steroidal anti-inflammatory drugs; (6) The patient refused.

Design outcomes

Primary

MeasureTime frame
Visual analogue score(VAS);Use of nonsteroidal analgesics in postoperative wards;

Secondary

MeasureTime frame
Intraoperative sufentanil dosage;Additional dose of sufentanil in resuscitation room;Use of nonsteroidal analgesics in postoperative wards;Postoperative complications;

Countries

China

Contacts

Public ContactLi Zhan

Lu’an Hospital of Anhui Medical University

zlhxq9090@163.com+86 159 5604 8010

Outcome results

None listed

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