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Comparison of the effects of bridging doses of hydromorphone and sufentanil on postoperative pain and outcomes in patients undergoing thoracoscopic surgery: A Multicenter, Randomized, Double-blind, Controlled Trial

Comparison of the effects of bridging doses of hydromorphone and sufentanil on postoperative pain and outcomes in patients undergoing thoracoscopic surgery: A Multicenter, Randomized, Double-blind, Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126932
Enrollment
Unknown
Registered
2026-06-18
Start date
2025-04-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Lung cancer

Interventions

Hydromorphone group:Intravenous injection of 0.015 mg/kg hydromorphone when closing the chest cavity
Sufentanil group:Intravenous injection of 0.15ug/kg sufentanil when closing the chest cavity

Sponsors

Shandong Provincial Hospital Affiliated to Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18 to 65 years old; 2. ASA levels I-III; 3.BMI 18~28 kg/m^2; 4.Patients undergoing elective general anesthesia thoracoscopy surgery; 5.Patients who have signed informed consent forms.

Exclusion criteria

Exclusion criteria: 1.History of mental illness, chronic pain, alcohol abuse, or long-term use of analgesics, sedatives, antidepressants, anxiolytics, and nonsteroidal anti-inflammatory drugs; 2.Severe liver and kidney dysfunction; 3.Allergic to relevant opioid drugs; 4.Use monoamine oxidase inhibitors, antidepressants, or antiepileptic drugs within 15 days before surgery; 5.Use sedatives, analgesics, or antiemetic drugs within 24 hours before surgery; 6.Pregnant or lactating women; 7.Patients who are not suitable for clinical research due to other reasons.

Design outcomes

Primary

MeasureTime frame
Postoperative VAS pain score;

Secondary

MeasureTime frame
Number of compressions of postoperative analgesia pump;Postoperative analgesic pump drug consumption;Remedial analgesia rate;Adverse reaction incidence rate;PACU wake-up time;Postoperative sleep quality;Postoperative emotional changes;The degree of interference of postoperative pain on activities;Postoperative incidence of pulmonary complications;Postoperative hospitalization days;Postoperative serum levels of IL-6 and IL-8;

Countries

China

Contacts

Public ContactWang Hongqian

Shandong Provincial Hospital Affiliated to Shandong First Medical University

taizi7576186@163.com+86 155 5412 1951

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026