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Clinical study of punctum reconstruction combined with canalicular stent in the treatment of punctum loss

Clinical study of punctum reconstruction combined with canalicular stent in the treatment of punctum loss

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050809
Enrollment
Unknown
Registered
2021-09-04
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-05-09

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

Conditions

Punctum loss

Interventions

Operation group:Punctum reconstruction

Sponsors

The Third Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
10 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with punctum loss caused by trauma, mass or punctum atresia who underwent punctum reconstruction; 2. The patient's condition has reached the surgical indication; 3. The patient has the ability of autonomy; 4. Patients can understand the procedures and methods of this study, voluntarily and strictly abide by the clinical study plan, complete this study, and voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Cases with incomplete clinical data; 2. Patients with severe nasal deformity, eye or nasal tumor; 3. Patients who cannot tolerate surgery.

Design outcomes

Primary

MeasureTime frame
Position of stent;Shape of reconstructed punctum;Mark score;

Secondary

MeasureTime frame
Lacrimal irrigation;

Countries

China

Contacts

Public ContactBai Fang

The Third Medical Center of Chinese PLA General Hospital

baifang@301hospital.com.cn+86 18618249879

Outcome results

None listed

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