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Application of tDCS in perioperative pain management in orthopedics

Application of tDCS in perioperative pain management in orthopedics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103937
Enrollment
Unknown
Registered
2025-06-09
Start date
2025-06-16
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Fracture

Interventions

test group:tDCS
control group:sham stimulation

Sponsors

The Third Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-65 years old, gender unlimited; 2.according to clinical symptoms, imaging diagnosis of long bone fracture and receiving orthopedic surgery; 3.there is no abnormal sensation, and it can normally express pain and other feelings; 4.before the test, fully understand the purpose and significance of the test, voluntarily follow the test process, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with communication and cognitive impairment who cannot cooperate; 2.History of previous head surgery or metal foreign body implantation; 3.Sensitive scalp; 4.Previous history of epilepsy; 5.Serious heart, lung, liver, kidney and other basic diseases, or unstable condition;

Design outcomes

Primary

MeasureTime frame
pain value;

Secondary

MeasureTime frame
Tenderness threshold;Analgesic drug dosage;

Countries

China

Contacts

Public ContactZhicheng Gao

The Third Affiliated Hospital of Xinxiang Medical University

13837317054@163.com+86 13837317054

Outcome results

None listed

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