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Effect of perioperative high-dose transdermal nicotine patch on pain sensitivity among male abstinent tobacco smokers undergoing thoracic surgery: A randomized controlled pilot study.

Effect of perioperative high-dose transdermal nicotine patch on pain sensitivity among male abstinent tobacco smokers undergoing thoracic surgery: A randomized controlled pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104070
Enrollment
Unknown
Registered
2025-06-10
Start date
2024-06-13
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

None listed

Interventions

Placebo control group:Routine anesthesia induction
Nicotine patch group:Nicotine patch 21mg/42mg - 21mg patch per 20 sticks, 40 cigarettes per day >= use 42mg dosage form patch

Sponsors

Henan Provincial People's Hospita,medical
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
25 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male, aged 25-70 years old, BMI between 18-28; 2.thoracoscopic lobectomy under general anesthesia; 3.American Society of Anesthesiologists (ASA) grade I-III; 4.regular smoking for more than 2 years, smoking more than 10 cigarettes per day in the past 6 months, and not successfully quitting smoking within 1 month, Fagerstrom score >=2 [34]; 5.No serious respiratory diseases, no serious cardiovascular and cerebrovascular diseases (hypertension is treated with SBP<=160mmHg, DBP<=90mmHg); 6. Obtain informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who have a history of alcoholism, long-term use of sedatives or analgesics; 2. Patients with psychiatric or neurological diseases (such as Parkinson's, depression, schizophrenia) and severe audio-visual dysfunction before surgery; 3.systolic blood pressure > 180 mmHg or diastolic blood pressure > 110 mmHg; 4. bleeding > 1000 ml or blood transfusion during surgery (participants bleeding more than 1000 ml or blood transfusion may be in a state of shock and require ventilation support after surgery, which may affect the outcome of postoperative pain assessment); 5.Patients who refuse to be treated with analgesic pumps.

Design outcomes

Primary

MeasureTime frame
Postoperative analgesic pump dosage;

Secondary

MeasureTime frame
Mechanical pain threshold;VAS score;Sleep quality score;Postoperative adverse events;Total length of hospital stay;

Countries

China

Contacts

Public ContactJiaqiang Zhang

Henan Provincial People's Hospita,medical

jqzhang@henu.edu.cn+86 13937121360

Outcome results

None listed

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