Randomized clinical trial on multimodal analgesia in fast-track surgery after single-incision video-assisted thoracoscopic lobectomy and segmentectomy

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-15007327

Enrollment

Unknown

Registered

2015-10-20

Start date

2016-01-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

lung cancer

Interventions

Parecoxib group:Parecoxib+intercostal nerve block

Patient-controlled analgesia group:Patient-controlled analgesia

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: After Institutional Ethic Committee approval and patient written consent120 patients will be enrolled 1. age ranging between 18-80 years old; 2. American Society of Anesthesiology (ASA) grade I-II; 3. scheduled to undergo anatomic lobectomy or segmentectomy and systematic lymphadenectomy with double lumen endotracheal intubation general anesthesia.

Exclusion criteria

Exclusion criteria: 1. ASA grade>=III; 2. cardiac disease such as coronary artery disease,myocardial infarction and arrhythmia; 3. cerebral vessel disease; 4. gastrointestinal disease such as peptic ulcer; 5. hepatic or renal disease; 6. coagulation disorders; 7. allergy to NSAIDS; 8. patient refusal.

Design outcomes

Primary

Measure	Time frame
medical recovery;Pain scales;	—

Secondary

Measure	Time frame
Postoperative stay,duration and cost of hospitalization;limb function;Opioids or other analgesic drugs consumption;the time of chest drainage and the total amount of chest drainage;	—

Countries

China

Contacts

Public ContactPeng Cha

bmyouyu@sina.com+86 18618373695

Outcome results

None listed

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