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Clinical study of modified floating needle technique for the treatment of acute pain after limb fracture surgery

Clinical study of modified floating needle technique for the treatment of acute pain after limb fracture surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000421
Enrollment
Unknown
Registered
2025-02-27
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Acute postoperative pain after extremity fracture

Interventions

test group:Modified Fu's Needle Therapy
control subjects:Oral celecoxib capsules

Sponsors

The General Hospital Of Western Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age between 1 8 and 6 0 years old and gender. (2) Patients with acute pain after limb fracture surgery (VAS = 5 points). (3) Meet the diagnostic criteria of Chinese and Western medicine diseases. (4) Those who agreed not to use other analgesic drugs during treatment and could tolerate modified floating needle therapy. (5) Informed, signed and voluntarily participated in the trial.

Exclusion criteria

Exclusion criteria: (1) Combined with serious primary diseases of the heart, liver, lungs, kidneys, brain and hematopoietic system. (2)Those with skin infection or necrosis around the operation opening. (3)Pregnant and lactating women. (4)Drug or alcohol abusers. (5)Those with open fracture or combined nerve injury. (6)Those with mental abnormality.

Design outcomes

Primary

MeasureTime frame
VAS pain score;—

Secondary

MeasureTime frame
swelling value;Assens Sleep Scale;—

Countries

China

Contacts

Public ContactDongfa Liao

The General Hospital Of Western Theater Command

861561462@qq.com13980733272

Outcome results

None listed

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