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Effect of silicone stent in endoscopic dacryocystorhinostomy

Comparison of Surgical outcome in endoscopic dacryocystorhinostomy with and without silicone stent: Hospital based study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070574
Enrollment
60
Registered
2024-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: H045- Stenosis and insufficiency of lacrimal passages

Interventions

Intervention1: Insertion of silicone stent in lacrimal sac: The study population will be divided into 2 groups of 30 each. Second group will undergo endoscopic dacryocystorhinostomy and silicone stent

Sponsors

Dr Mukesh Verma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with chronic dacryocystitis. Age more than 18 years.

Exclusion criteria

Exclusion criteria: Patient not giving consent Age less than 18 years Revision cases of endoscopic DCR suspicion of malignancy

Design outcomes

Primary

MeasureTime frame
To observe the patency of lacrimal sac after endosopic DCR with silicone stent and without stentTimepoint: 1week, 3 week, 6 week and 10 week and 6month—

Secondary

MeasureTime frame
Observe synechiae formation after and other complication of endoscopic DCR with silicone stent and without stentTimepoint: 1week, 3 week, 6 week and 10 week and 6month—

Countries

India

Contacts

Public ContactDr Mukesh Verma

Government Medical College, Haldwani

Drshahzadjnmch85@gmail.com9634623901

Outcome results

None listed

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