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. 2020 Apr 7;2020(4):CD012309. doi: 10.1002/14651858.CD012309.pub2

Qiu 2000.

Methods Study design: randomized controlled trial, parallel group
Unit of analysis: eyes
Number randomized: 92 in total, 48 to the MMC group, 44 to the DCR alone group
Number of arms: 2
Enrollment start year: 1995
Length of follow‐up: 29 months
Sample size calculations: not reported
Losses to follow‐up: none
Participants Country: China
Age (mean (SD)): 29.6 (NR) in total
Females (n (%)): 82 (89) in total
Inclusion criteria: patients with chronic dacryocystitis
Exclusion criteria: patients with upper lacrimal duct or nasal disorders, other systemic disorders
Study group differences: no difference
Interventions Intervention: DCR with application of 0.4 mg/mL MMC
Comparison intervention: DCR alone
Outcomes Measured outcomes:
  • functional success, defined as the relief of epiphora

  • anatomic success, defined as patency to lacrimal irrigation


Adverse events: anastomotic bleeding
Identification Author name: SK Qiu
 Institution: Department of Ophthalmology, Tengzhou Central Hospital
Email: not reported
Notes Funding source: not reported
Declarations of interest: not reported
Trial registration number: not reported
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Random sequence generation was not reported.
Allocation concealment (selection bias) Unclear risk Method of treatment allocation concealment was not reported.
Blinding of participants and personnel (performance bias) 
 All outcomes Unclear risk Masking of study participants and investigators was not reported.
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk Masking of outcome assessors was not reported.
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No missing data, participants were analyzed in the group to which they had been randomized.
Selective reporting (reporting bias) Unclear risk No trial or protocol registration available for comparison to ascertain selective outcome reporting.
Other bias Unclear risk There was insufficient information to permit a judgement of 'low risk' or 'high risk'.