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The Lidocaine Cataplasms for Preventing Chronic Post-thoracotomy Pain: A Prospective, Multicenter,Randomized Controlled Trial

The Lidocaine Cataplasms for Preventing Chronic Post-thoracotomy Pain: A Prospective, Multicenter,Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093171
Enrollment
Unknown
Registered
2024-11-29
Start date
2022-10-28
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Chronic Post-thoracotomy Pain

Interventions

Test group:The test group was treated with oral celecoxib capsule 0.2 g, Q12 h in combination with Lidocaine Cataplasms
Control group:Patients in the control group were given oral celecoxib capsule 0.2 g, Q12 h

Sponsors

NanJing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1)Age greater than or equal to 18 years, less than 80 years, gender-neutral; 2)Grade A healing of surgical incisions; 3)Pain is mainly confined to the peri-incision area, with NRS >= 4 at 1 week postoperatively; 4)Those whose cause of pain is primarily somatic rather than psychosomatic; 5)Expected survival >= 3 months.

Exclusion criteria

Exclusion criteria: 1) Allergy to nonsteroidal, amide local anesthetics or skin hypersensitivity to lidocaine patches; 2) History of continuous use of analgesic medication for 2 weeks prior to surgery; 3) Presence of pain other than incisional pain and need for analgesic medication other than the study medications; 4) The patient has a history of severe hepatic or renal function, cardiac insufficiency, gastrointestinal disorders such as creatinine >= 2 times the high limit of normal or ALT or AST >= 2.5 times the high limit of normal, Child C grade of hepatic function, or gastrointestinal perforation or obstruction; 5) Subject has a history of alcohol abuse, drug abuse; 6) Presence of depression and anxiety, inability to communicate verbally; cognitive deficits or mental illness; or other causes of impaired consciousness; 7) Patients who are unable to follow the study plan and visit schedule; 8) Participation in other clinical trials within 3 months prior to trial; 9) Pregnant and lactating women; 10) Those who, in the opinion of the researcher, cannot be enrolled for any reason whatsoever.

Design outcomes

Primary

MeasureTime frame
numerical rating scale;

Secondary

MeasureTime frame
Douleurneuropathique 4 questions;daily sleep interference score;Analgesic drug use;

Countries

China

Contacts

Public ContactXu Chenjie

Nanjing First Hospital

xcj2001@163.com+86 139 5180 9998

Outcome results

None listed

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