CClinicalTrials.gg
CompletedNCT05586620Updated Oct 19, 2022

3 Snip Punctoplasty With and Without Mitomycine C.

An interventional study of 3-snip punctoplasty and 3-snip punctoplasty and Mitomycin C in Punctal Stenosis, sponsored by Al-Azhar University. Completed at 1 site in Egypt. Open to participants aged 16 Years to 63 Years. Per ClinicalTrials.gov, last updated 2022-10-19.

Sponsored by Al-Azhar University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Jun 2021, registered Oct 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Non-randomized
Ages
16 Years to 63 Years
Sex
All
01

Study summary

Punctal stenosis is a progressive constriction of the puncta with resultant epiphora. One of the most effective treatment options is 1- to 4-snip punctoplasty combined with or without Mitomycin-C.

02

Conditions studied

  • Punctal Stenosis
03

In context

Constriction, Pathologic

1,117 studies on the registry are indexed under Constriction, Pathologic; 231 are open to participants now.

This study's enrollment of 18 is below the median of 80 across 672 interventional studies indexed under Constriction, Pathologic.

Browse Constriction, Pathologic studies →

Lead sponsor

Al-Azhar University is the lead sponsor of 505 studies on the registry; 167 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 63 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with recurrence of punctal stenosis at the end of 1 month following punctal dilatation.

Exclusion criteria

Exclusion Criteria:

  • patients with associated lacrimal passage obstruction
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
18 participants (actual)

Study arms

  • Active comparator
    3-snip punctoplasty

    Procedure: 3-snip punctoplasty

  • Active comparator
    3-snip punctoplasty with mitomycin C

    Procedure: 3-snip punctoplasty and Mitomycin C

Interventions

  • Procedure3-snip punctoplasty

    punctoplasty, more commonly known as watery eye surgery, is an ophthalmic surgical procedure performed to correct punctal stenosis (a condition that causes tears to overflow from the eyes) by widening the punctal opening to allow the tears to drain with ease.

  • Procedure3-snip punctoplasty and Mitomycin C

    punctoplasty, more commonly known as watery eye surgery, is an ophthalmic surgical procedure performed to correct punctal stenosis (a condition that causes tears to overflow from the eyes) by widening the punctal opening to allow the tears to drain with ease. Mitomycin C is a chemotherapeutic agent that acts by inhibiting DNA synthesis

06

What researchers measure

Primary outcomes

  1. Punctal patency

    Punctum will be assessed by inspection of the lid by slitlamb examination, whither obstructed or not

    Time frame: Baseline

  2. Punctal patency

    Punctum will be assessed by inspection of the lid by slitlamb examination, whither obstructed or not

    Time frame: 1 week postoperative

  3. Punctal patency

    Punctum will be assessed by inspection of the lid by slitlamb examination, whither obstructed or not

    Time frame: 1 month postoperative

  4. Punctal patency

    Punctum will be assessed by inspection of the lid by slitlamb examination, whither obstructed or not

    Time frame: 3 months postoperative

  5. Presence of Epiphora

    It will be assessed by inspection of the lid by slitlamb examination.

    Time frame: Baseline

  6. Presence of Epiphora

    It will be assessed by inspection of the lid by slitlamb examination.

    Time frame: 1 week postoperative

  7. Presence of Epiphora

    It will be assessed by inspection of the lid by slitlamb examination.

    Time frame: 1 month postoperative

  8. Presence of Epiphora

    It will be assessed by inspection of the lid by slitlamb examination.

    Time frame: 3 month postoperative

07

Study locations

1 site
  • Ehab tharwat
    Damieta, New Damietta 34517, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 19, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05586620
Lead sponsor
Al-Azhar University
Responsible party
Ehab tharwat (Principal investigator, Al-Azhar University) — Principal investigator
First posted
Oct 19, 2022
Start date
Jun 1, 2021
Primary completion
Jun 1, 2022
Completion
Jun 10, 2022
Last update
Oct 19, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion