Skip to content

Non-Invasive Surgery of conjunctivochalasis Using Plasma.

Evolution of plasma assistant non-invasive surgery (PANIS) in conjunctivochalasis treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181229042160N3
Enrollment
6
Registered
2019-01-13
Start date
2018-11-22
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Conjunctivochalasis. Conjunctivochalasis

Interventions

Surgery begins at a distance of 4 mm from the inferior limbus of the eye
The number of plasma spots varies depending on the degree of conjunctivochalasis progression
If the conjunctivochalasis is grade 2, two rows of spots are placed at a distance of 4 mm of the limbus next to each other
If the conjunctivochalasis is grade 3, depending on the severity of the disorder two to four spots are placed without any gaps next to each other at a distance of 4 mm of the limbus
Also, if the conjunctivochalasis is in the nasal side (towards the nose) or laterally (toward the ear), the spots will be in the 4 mm of the same point in the semicircle, but if there is a conjunctivo

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to No maximum

Inclusion criteria

Inclusion criteria: Tearing and redness of the eye Dry eye Eye irritation Itchy eyes The sensation of having foreign body in the eye

Exclusion criteria

Exclusion criteria: Having systemic and eye diseases Having inflammatory eye diseases such as ocular cicatricial pemphigoid (OCP) History of conjunctival surgery Having entropion and ectropion disorders History of retinal surgery and glaucoma Having distichiasis

Design outcomes

Primary

MeasureTime frame
Grading of conjunctivochalasis. Timepoint: Before surgery and one day, one week, one month, three months and six months after surgery. Method of measurement: Slit-lamp examination.;Tear break up time (TBUT). Timepoint: Before surgery and one day, one week, one month, three months and six months after surgery. Method of measurement: Slit-lamp examination and fluorescine strip.;Corneal staining zones. Timepoint: Before surgery and one day, one week, one month, three months and six months after surgery. Method of measurement: Slit-lamp examination and fluorescine strip.

Secondary

MeasureTime frame
Schirmer test. Timepoint: Before surgery and one day, one week, one month, three months and six months after surgery. Method of measurement: Schirmer paper.;Tear meniscus height. Timepoint: Before surgery and one day, one week, one month, three months and six months after surgery. Method of measurement: Slit-lamp examination.;Uncorrected visual acuity (UCVA). Timepoint: Before surgery and one day, one week, one month, three months and six months after surgery. Method of measurement: Eye exam by optometrist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarhad Nejat

Semnan University of Medical Sciences

fanejat@yahoo.com+98 23 3344 1022

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026