Skip to content

Evaluation of intra ocular pressure following intubation

A Comparison and Evaluation of intra ocular pressure following intubation with Mccoy, Macintosh and video laryngoscope (Glide scope) in patients with cataract surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201301079585N3
Enrollment
180
Registered
2013-02-21
Start date
2012-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

cataract. Cataract, unspecified

Interventions

Intervention 1: Intubation by Mccoy laryngoscope made by Riester company of Germany, after induction of anesthesia. Intervention 2: Intubation by Macintosh laryngoscope made by Riester company of Germ
Treatment - Devices
Intubation by Mccoy laryngoscope made by Riester company of Germany, after induction of anesthesia.
Intubation by Macintosh laryngoscope made by Riester company of Germany, after induction of anesthesia.
Intubation by glidescope made by Verathon® Medical (Canada) ULC, after induction of anesthesia.

Sponsors

Vice Chancellor for research, Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria are: patients who are admitted for elective cataract surgery, age: 20-70 and have ASA classification as 1 or 2. Exclusion criteria are: history of alcohol and drug abuse, antihypertensive and cardiovascular medicines usage, glaucoma eye drop usage, diabetes and open eye injuries.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intra ocular pressure. Timepoint: before and after intubation, and 5 minutes later. Method of measurement: Schiotz tonometer.

Secondary

MeasureTime frame
Mean Arterial Pressure. Timepoint: Before and after intervention and every 5 minutes during operation. Method of measurement: mmhg / by electronic monitoring.;Heart Rate. Timepoint: Before and after intervention and every 5 minutes during operation. Method of measurement: electronic monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSyavash Moradi

Kerman University of Medical Sciences

javakrd34@gmail.com+98 34 1226 3815

Outcome results

None listed

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