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Vasopressin for Abdominal Compartment Syndrome

N/A
Waitlist Available
Research Sponsored by The Cleveland Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights

Study Summary

This trial looks at the relationship between increased pressure in different parts of the body andfindings in urine and blood.

Who is the study for?
This trial is for adults aged 18-72 who qualify for bariatric surgery and are undergoing laparoscopic sleeve gastrectomy. It's not suitable for those under 18, with other causes of increased abdominal or chest pressure besides obesity, urinary infections, eye conditions/surgery, lung diseases, neurological diseases, or very high surgical risk (ASA class IV/V).Check my eligibility
What is being tested?
The study aims to understand the relationship between elevated pressures in the abdomen and chest (due to PEEP) and brain pressure. It also examines how these pressures affect vasopressin release, urine production, and concentration levels at different times.See study design
What are the potential side effects?
While specific side effects aren't listed here as it's an observational study on physiological responses rather than a drug trial; potential risks may include discomfort from increased pressure measurements.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 hours for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Physiologic variations secondary to pneumoperitoneum

Trial Design

1Treatment groups
Experimental Treatment
Group I: Study ArmExperimental Treatment1 Intervention
Measurements of optic nerve diameter, Urine and plasma osmolality, Serum vasopressin.

Find a Location

Who is running the clinical trial?

The Cleveland ClinicLead Sponsor
1,026 Previous Clinical Trials
1,366,060 Total Patients Enrolled

Media Library

Intraabdominal Pressure Elevation Clinical Trial Eligibility Overview. Trial Name: NCT03707054 — N/A
Abdominal Compartment Syndrome Research Study Groups: Study Arm
Abdominal Compartment Syndrome Clinical Trial 2023: Intraabdominal Pressure Elevation Highlights & Side Effects. Trial Name: NCT03707054 — N/A
Intraabdominal Pressure Elevation 2023 Treatment Timeline for Medical Study. Trial Name: NCT03707054 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals below the age of sixty allowed to partake in this research?

"The eligibility for this clinical trial necessitates that participants are within the 18 to 72 age group. There are 5 trials specifically targeting juveniles, and 27 dedicated to seniors."

Answered by AI

Is it possible to participate in this clinical examination?

"To partake in this trial, candidates must be between 18 to 72 years old and diagnosed with intracranial hypertension. A total of 16 participants are being sought for the study."

Answered by AI

Are there still vacancies for participating in this experiment?

"This research endeavour, according to the information hosted on clinicaltrials.gov, is no longer recruiting participants. Initially posted in April of 2017 and last updated in July of 2022, this project has now closed its doors to new candidates; however, 31 other studies are still searching for volunteers at present."

Answered by AI
~2 spots leftby Apr 2025