Skip to content

A prospective randomized controlled study on the effectiveness of intraoperative precision ligation in preventing salivary fistula after parotidectomy

A prospective study on the effectiveness of intraoperative precision ligation in preventing salivary fistula after parotidectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035311
Enrollment
Unknown
Registered
2020-08-07
Start date
2020-08-04
Completion date
Unknown
Last updated
2020-08-10

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

Conditions

Salivary fistula after parotidectomy

Interventions

Intraoperative precision ligation group:Precise ligation of the parotid duct during surgery
Control group:Routine parotid stump suture

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The patient is completely voluntary and has the ability to sign the research informed consent before joining the research; 2, aged ? 18 years old and ? 70 years; 3. The preoperative examination is diagnosed as a unilateral benign tumor of the superficial parotid gland, and surgical treatment is planned; 4. High compliance, able to complete research.

Exclusion criteria

Exclusion criteria: 1. History of head and neck radiotherapy; 2. Symptoms of dry mouth; 3. History of other salivary gland diseases; 4. Recurrent parotid gland tumors; 5. History of trauma to the affected parotid gland area; 6. History of surgery on the affected parotid gland area; 7. Bilateral parotid gland tumors; 8. Blood coagulation dysfunction; 9. Women during pregnancy or breastfeeding; 10. History of serious systemic diseases.

Design outcomes

Primary

MeasureTime frame
rate of salivary fistula;

Secondary

MeasureTime frame
rate of facial nerve palsy;

Countries

China

Contacts

Public ContactZhang Dongsheng

Shandong Provincial Hospital

ds63zhang@163.com+86 15168887559

Outcome results

None listed

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