Clinical Trials Directory

Trials / Unknown

UnknownNCT03590873

The Effect of Restrictive Fluid and Vasopressin During Surgery of Burn Patients

The Effect of Restrictive Fluid and Vasopressin During Surgery of Burn Patients: a Randomized Clinical Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
158 (estimated)
Sponsor
Hangang Sacred Heart Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a randomized double-blinded study to investigate in which the groups are designated as the control group and the restrictive group to further evaluate significant differences in intraoperative blood loos during burn surgery.

Detailed description

This is a randomized double-blinded study to investigate the effect of fluid restriction and vasopressin on blood loss during surgery of the burn patients. The groups are designated as the control group and the restrictive group to further evaluate significant differences in intraoperative blood loss during the surgery.

Conditions

Interventions

TypeNameDescription
DRUGVasopressinVasopressin, is a hormone synthesized as a peptide prohormone in neurons in the hypothalamus, and is converted to arginine vasopressin. It then travels down the axon of that cell, which terminates in the posterior pituitary, and is released from vesicles into the circulation in response to extracellular fluid hypertonicity (hyperosmolality). Arginine vasopressin has two primary functions. First, it increases the amount of solute-free water reabsorbed back into the circulation from the filtrate in the kidney tubules of the nephrons. Second, arginine vasopressin constricts arterioles, which increases peripheral vascular resistance and raises arterial blood pressure.

Timeline

Start date
2018-07-25
Primary completion
2019-06-04
Completion
2019-06-04
First posted
2018-07-18
Last updated
2018-07-31

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03590873. Inclusion in this directory is not an endorsement.