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Changes of Intra Abdominal Pressure During Surgeries in Prone Position as a Marker of Renal Damage

Intraoperative Abdominal Pressure Measurement in Patients Undergoing Spine Surgeries in Prone Position as a Marker of Renal Damage

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05626868
Enrollment
24
Registered
2022-11-25
Start date
2021-05-01
Completion date
2022-12-31
Last updated
2022-11-25

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

Conditions

Intraabdominal Hypertension, Prone Postion, Spine Surgery

Brief summary

Background: Patients undergoing surgical operations in prone position do not have a measure of intra abdominal pressure as a standard procedure. Many of them could have elevated values of this parameter and could be exposed to possible renal damage due to a stiffening of the abdominal muscles while being positioned prone. Purpose of study: Intraoperative intrabdominal pressure measurement and evaluation of correlation with possible postsurgical complications. Methodology: Electronic device able to measure intra abdominal pressure is connected between a Foley catheter and a urinary collecting bag. During the procedure, values of the intra abdominal pressure are displayed on a monitor next to anaesthetic machine in real time. The numbers representing the pressure in mmHG are assessed and recorded. Discussion: Possible correlation between intra abdominal hypertension and postsurgical complications in patients operated in prone position could be a foundation to further clinical trials and presurgical assessment of intraabdominal pressure.

Interventions

DEVICEIntra abdominal pressure measurement

Device: Biometrix - Intraabdominal pressure monitoring set Intraabdominal pressure monitoring with the intended set in values of milimeters of mercury (mmHg) in real time.

Sponsors

Medical University of Warsaw
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Consent to participate in the study * Patients qualified for surgical stabilization of the spine in prone position

Exclusion criteria

* No consent to participate in the study or inability to obtain consent * The inability to insert a urinary catheter * No indication for urinary catheter * Patients undergoing palliative treatment * Patients with advanced liver and kidney disease

Design outcomes

Primary

MeasureTime frameDescription
Increase in intra abdominal pressure during surgery.IntraoperativeChange in intra abdominal pressure during surgery in prone position.

Secondary

MeasureTime frameDescription
Correlation of increased abdominal pressure with renal dysfunction assessed by creatinine.From start to eight hours after the surgery.Assessment of renal function in labolatory tests: creatinine change (mg/dl).
Correlation of increased abdominal pressure with renal dysfunction assessed by urea.From start of surgery to eight hours after the surgery.Assessment of renal function in labolatory tests: urea change (mg/dl).
Correlation of increased abdominal pressure with renal dysfunction assessed by potassium.From start of surgery to eight hours after the surgery.Assessment of renal function in labolatory tests: potassium change (mg/dl).
Correlation of increased abdominal pressure with mioglobin.From start of surgery to eight hours after the surgery.Assessment in labolatory tests: mioglobin change (mg/dl).

Countries

Poland

Contacts

Primary ContactBartosz Stangiewicz, MD
bartosz.stangiewicz@wum.edu.pl+48605941973

Outcome results

None listed

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