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Influence of Perioperative Fluid Management on Intraocular Pressure During Hynecologic Laparoscopic Pelvic Surgery

Influence of Perioperative Fluid Management on Intraocular Pressure During Hynecologic Laparoscopic Pelvic Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01676064
Enrollment
50
Registered
2012-08-30
Start date
2012-08-31
Completion date
Unknown
Last updated
2012-08-30

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

Conditions

Influence of Perioperative Fluid Regime on Intraocular Pressure During Laparoscopic Gynecologic Surgery

Keywords

intraocular pressure, perioperative fluid, trendelenburg position, laparoscopic gynecologic surgery

Brief summary

The aim of this study was to quantify the Intraocular Pressure (IOP) changes in patients undergoing laparoscopic hysterectomy at different time points and body positions throughout the procedure, and to explore the influence of perioperative fluid management on the fluctuations of IOP during perioperative period.

Interventions

OTHERrestrictive fluid regime

Sponsors

Ziv Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* 50-60 adult female patients, * ASA physical status I or II, * scheduled for elective hynecologic laparoscopic pelvic surgery will be included in the study.

Exclusion criteria

* patients will be excluded if they are \> 70 and \< 18 yr of age, * had have a body weight \> 150% of their ideal body weight, * have acute or chronic eye disease, * receive any medication known to alter IOP, or * have any mental illnesses.

Design outcomes

Primary

MeasureTime frame
measurements of intraocular pressure during laparoscopic gynecologic surgery a sa function of diffrent perioperative fluid regimes.24 hr
IOP will be measured using a Tono-pen® XL by an ophthalmologist who will be unaware of the perioperative fluid administration regimen.24 hr

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026