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Evaluation of the efficacy of single-port thoracoscopic postoperative sutureless double thin tube catheterization versus traditional catheterization on rapid postoperative recovery: a prospective, single-center, randomized, double-blind, parallel, controlled study

Evaluation of the efficacy of single-port thoracoscopic postoperative sutureless double thin tube catheterization versus traditional catheterization on rapid postoperative recovery: a prospective, single-center, randomized, double-blind, parallel, controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070654
Enrollment
Unknown
Registered
2023-04-19
Start date
2023-04-22
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

lung carcinoma

Interventions

Control group:Conventional tube placement for single hole thoracoscopy (TTD)
Treatment group:Double tubing without suturing after Uniportal thoracoscopy

Sponsors

Department of thoracic surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. age at 18-75; 2. no selection on gender; 3. peripheral lung nodule; 4. diameters of nodule <3cm; 5. diagnosis of lung carcinoma; 6. lobes or segments resection + lymph node dissection, by VATS; 7. agree to the study;

Exclusion criteria

Exclusion criteria: 1. Patients with incomplete perioperative medical records; 2. Patients undergoing thoracotomy due to pleural atresia or hemorrhage during VATS operation; 3. Patients with VATS pneumonectomy or wedge-shaped resection; 4. Pulmonary tuberculosis, severe pneumonia, bronchiectasis and other chronic lung diseases; 5. Preoperative combination of malignant tumors in other sites (not including cured); 6. Complicated with serious diseases of heart, lung, kidney, brain, blood and neuropsychiatric system; 7. Poorly controlled hypertension or other systemic diseases; 8. Patients with indwelling chest tube due to pneumothorax or pleural effusion before surgery; 9. Multiple lesions require simultaneous surgery; 10. Severe coagulation dysfunction; 11. Hypoproteinemia (ALB < 25g/L) and severe malnutrition; 12. Patients who have received neoadjuvant chemoradiotherapy before surgery; 13. Patients not appropriate in this study judged by researcher.

Design outcomes

Primary

MeasureTime frame
NRS/VAS score;postoperative volume of drainage;the period of post-operative chest tube drainage;

Secondary

MeasureTime frame
analgesic consumption;intraoperative bleeding;sleep quality scores;Self-Rating Anxiety Scale;post-operative stays;nflammatory cytokines;lung recruitment;complications;re-catheterization rate;the incision healing rate;

Countries

China

Contacts

Public ContactDongxin Hu

Provincial Hospital Affiliated to Shandong First Medical University

hudx312@163.com+86 15168866711

Outcome results

None listed

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