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Vasopressin in Intraabdominal Pressure Elevation

NeuroTherapia, Inc. logo

NeuroTherapia, Inc.

Status

Completed

Conditions

Intracranial Pressure Increase
Abdominal Compartment Syndrome

Treatments

Diagnostic Test: Study Arm

Study type

Interventional

Funder types

Other

Identifiers

NCT03707054
FLA 17-031

Details and patient eligibility

About

The aim of this study is to investigate any direct correlation between increased intrathoracic pressure, intraabdominal pressure and intracranial pressure, following a controlled elevation in intraabdominal pressure and intrathoracic pressure (PEEP). The second end-point is to investigate any correlation between elevated intracranial pressure and vasopressin release, urine output and urine and serum osmolality by measuring their values at different time-points.

Full description

Increase in intraabdominal pressure (IAP) has been demonstrated to correlate with consequential hemodynamic effects. Several studies have been carried out mostly in experimental settings to define the underlying mechanisms that regulate the pathophysiology following an increase in IAP. In the last years this topic has become concerning because of the wide spread of laparoscopy, that is namely an iatrogenic acute increase in IAP.

Patients selected and consented for elective surgery will undergo standard of care and additional measurements during and after surgery. The measurements will be done at different stages of laparoscopic surgery.

  1. A) Baseline, patient under general anesthesia, Foley catheter positioned, beginning urine collection, before insufflation of pneumoperitoneum
  2. B) 10-15 minutes after insufflation of pneumoperitoneum at 15mmHg, PEEP at 5cmH2O or lowest setting
  3. C) 10-15 minutes after stabilization of PEEP at 10cmH2O, pneumoperitoneum still at 15 mmHg
  4. D) 10-15 minutes after desufflation of pneumoperitoneum and basal mechanical ventilation

Measurements include :

  • Intraabdominal pressure IAP: assessed via laparoscopic insufflator, set at 15 mmHg as a standard value for all laparoscopic procedures
  • Intrathoracic pressure: indirectly measured by variability of peak expiratory pressures
  • Urine collection: through a Foley catheter from the beginning of surgery to post-operative day 1
  • Urine osmolality (to be assessed at set time-points )
  • Hourly urine output (at least 24 hours in order to evaluate expected significant variation even after the procedure end, since renal adaptation could take longer period)
  • Serum/plasma collection : blood draws to evaluate specific values of
  • Plasma Vasopressin (ADH)
  • Serum osmolality
  • Mean arterial pressure : standard of care
  • Pulmonary expiratory end-pressure (PEEP): anesthesiologists routinely adapt PEEP in order to maintain an optimal ventilation, especially in obese patients and during laparoscopy
  • Optic nerve sheath diameter (ONSD): a 7.5-MHz linear ultrasound probe to measure the diameter of the optic nerve sheath 3 mm behind the globe is going to be used; a trained study personnel physician will take the non-invasive sonographic picture using ultrasound. The ONSD will be measured from the captured picture. Study personnel will record the interaction on the patient's chart and include the measurement on the database

Enrollment

16 patients

Sex

All

Ages

18 to 72 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18-72
  • Patients meeting NIH criteria for bariatric surgery
  • Patients undergoing laparoscopic sleeve gastrectomy

Exclusion criteria

  • • Age below 18 years

    • American Society of Anesthesiologist (ASA) class IV or V
    • Other evident/diagnosed causes of increased IAP or increased intrathoracic pressure, except for obesity
    • Active urinary tract infection
    • Previous or concomitant neurological disease
    • Previous or concomitant ophthalmic conditions/eye surgery
    • Previous or concomitant lung diseases

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

16 participants in 1 patient group

Study Arm
Experimental group
Description:
Measurements of optic nerve diameter, Urine and plasma osmolality, Serum vasopressin.
Treatment:
Diagnostic Test: Study Arm

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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