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NCT04585217 · ClinicalTrials.gov registry record · NA
A Comparison of the Effect of Suture Material on Blepharoplasty Incision
A NA study, sponsored by Massachusetts Eye and Ear Infirmary.
- Completed
- Registry status
- NA
- Development phase
- 23
- Enrollment target
NCT04585217 is a NA study that has completed, run by Massachusetts Eye and Ear Infirmary. The registered enrollment target is 23 participants.
The verdict
NCT04585217, a NA study, has completed, sponsored by Massachusetts Eye and Ear Infirmary.
- COMPLETED
- Registry status
- NA
- Development phase
- 23 participants
- Enrollment target
Study Summary
The objective is to compare the effect of suture material on blepharoplasty incision. Outcomes of blepharoplasty scar and/or cosmesis will be compared between plain gut and polypropylene suture. Additionally, the study will assess whether certain Fitzpatrick skin types are associated with increased rates of poor outcomes after blepharoplasty.
Interventions
- PROCEDURE Randomized laterality of suture materials for closure (6-0 polypropylene monofilament suture vs fast absorbing gut suture on right eyelid)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2020-05-30 |
| Est. Completion | 2022-06-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04585217
The ClinicalTrials.gov registry entry for NCT04585217 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Massachusetts Eye and Ear Infirmary, which has 73 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Randomized laterality of suture materials for closure (6-0 polypropylene monofilament suture vs fast absorbing gut suture on right eyelid) is the first listed.
NCT04585217 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04585217 about?
NCT04585217 is a clinical study titled "A Comparison of the Effect of Suture Material on Blepharoplasty Incision". The objective is to compare the effect of suture material on blepharoplasty incision. Outcomes of blepharoplasty scar and/or cosmesis will be compared between plain gut and polypropylene suture. Additionally, the study will assess whether certain Fitzpatrick skin types are associated with increased ...
What is the current status of trial NCT04585217?
This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2020-05-30. Estimated completion is 2022-06-30.
What interventions are being tested in trial NCT04585217?
The interventions under investigation include: Randomized laterality of suture materials for closure (6-0 polypropylene monofilament suture vs fast absorbing gut suture on right eyelid) (PROCEDURE).
Who is sponsoring clinical trial NCT04585217?
This trial is sponsored by Massachusetts Eye and Ear Infirmary, which has 73 total clinical trials registered on ClinicalTrials.gov.
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