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Prospective randomized study of silicone stent intubation in endoscopic dacryocysto-rhinostomy for acquired nasolacrimal duct obstruction - SEND study

Prospective randomized study of silicone stent intubation in endoscopic dacryocysto-rhinostomy for acquired nasolacrimal duct obstruction - SEND study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000721
Enrollment
Unknown
Registered
2008-04-24
Start date
2006-04-05
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

Acquired nasolacrimal duct obstruction

Interventions

Two groups:endoscopic dacryocysto-rhinostomy, Stenting: 8 weeks or no stent at all Follow-up: 26 weeks. versus Endoscopic dacryocystorhinostomy with or without eight weeks bicanalicular silicone intub

Sponsors

None listed

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adult patients (>18) with NLDO (on table finding); 2. Informed consent; 3. Follow-up to 6 months; 4. No previous lacrimal surgery; 5. No concomitant canalicular disease; 6. Agree for randomization

Exclusion criteria

Exclusion criteria: 1. Previous dacryocystorhinostomy; 2. Canalicular obstruction requiring membranectomy after sac exposure for free passage of Bowman probe; 3. Requiring concomitant punctoplasty procedure

Design outcomes

Primary

MeasureTime frame
% of success achieved in each group at postoperative six months % with formation of granulation tissue at rhinostomy site, time course, response to local debridement and nasal steroid spray;

Secondary

MeasureTime frame
Risk factors analyses for surgical failure or persistence of symptom (age, gender, duration of symptom preoperatively, postoperative tube prolapse, presence of granulation tissue around internal ostium, difficulty intraoperative hemostasis, surgeon's immediate impression, level of surgical experience, endoscopist's assessment postoperatively);Risk factors analyses for surgical failure or persistence of symptom (age, gender, duration of symptom preoperatively, postoperative tube prolapse, presence of granulation tissue around internal ostium, difficulty intraoperative hemostasis, surgeon's immediate impression, level of surgical experience, endoscopist's assessment postoperatively);

Countries

China

Contacts

Public ContactDr. Kelvin K.L.Chong
chongkamlung@gmail.com+852 2632-2878

Outcome results

None listed

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