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Effect of oral pregabalin on postoperative sleep in patients undergoing video-assisted thoracoscopic surgery: a prospective, randomized controlled trial.

Effect of oral pregabalin on postoperative sleep in patients undergoing video-assisted thoracoscopic surgery: a prospective, randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071850
Enrollment
Unknown
Registered
2023-05-26
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Pulmonary nodules

Interventions

75mg pregabalin group:On the night of operation, the morning and evening of the first and second day after operation, one pregabalin capsule (75mg) and one placebo with the same shape and smell were t
150mg pregabalin group:On the night of operation, the morning and evening of the first and second day after operation, two pregabalin capsules (150mg) were taken orally
control group:On the night of operation, the morning and evening of the first and second day after operation, two placebos with the same shape and smell were taken orally

Sponsors

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1?Age 18-65 years old; 2? ASA?-?, BMI18-30 kg/?; 3?Elective VATS;

Exclusion criteria

Exclusion criteria: ? Unilateral pneumonectomy; ? There was sleep disorder before operation (Pittsburgh Sleep Quality Index score > 5). ? Taking sedatives and antidepressants for more than 3 months; ? allergic to pregabalin; ? Patients with abnormal liver and kidney function before operation; ? Drug and alcohol dependence; ? Failure to communicate normally: hearing impairment, language comprehension impairment, mental illness, etc. ? Unable to understand the content of the scale and refused to participate.

Design outcomes

Primary

MeasureTime frame
Incidence of sleep disorder on the night of operation;

Secondary

MeasureTime frame
AIS score;SMH score ;PSQI ;NRS score of surgical shoulder and incision;Ramsay ;Patient satisfaction score;

Countries

China

Contacts

Public ContactZhao Linlin

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University

lin1675@163.com+86 181 6877 7313

Outcome results

None listed

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