Direct Peritoneal Resuscitation for Intra-abdominal Catastrophes

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05208489

Enrollment

108

Registered

2022-01-26

Start date

2021-12-16

Completion date

2023-06-30

Last updated

2022-01-26

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

Conditions

Intestinal Obstruction, Intestinal Perforation, Trauma Abdomen

Brief summary

It is a retrospective study. Patients, who presented with either traumatic or general surgery emergencies, undergone exploratory laparotomy, had an open abdomen management and received Direct Peritoneal Resuscitation in addition to standard resuscitation will be considered as meeting the criteria to collect the data.

Detailed description

Due to the high volume of patient transfers from different facilities with difficult intra-abdominal pathologies and the high case-mix index at Westchester Medical Center, we see many patients who require re-operations and open abdominal management. Since July1st of 2020 we have been using DPR in addition to standard iv fluids on all patients who undergo open abdominal management and it is now standard of care at our facility. we plan to collect the data from all qualified subjects who received DRP since 7/1/2020 to 6/30/2022.

Interventions

OTHERthere is no intervention involved in this study

there is no intervention involved in this study.

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Adult patients 18 years of age or older. * Trauma or General surgery patients who undergo emergency abdominal surgery via laparotomy and who had open abdominal management during the index procedure at our institution. * Patients who are transferred to our institution with an already open abdomen will also be eligible if they required continued open abdominal management.

Exclusion criteria

* Patients \<18 years are excluded.

Design outcomes

Primary

Measure	Time frame	Description
Post operative outcomes	through out the hospitalization and 30 days after discharge.	intra abdominal infections and other complications

Secondary

Measure	Time frame	Description
length of hospital stay	post procedure to 30 days after discharge.	includes ICU stay, ventilator days and mortality.

Countries

United States

Contacts

Primary ContactAnuritha Tirumani, MBBS

anuritha.tirumani@wmchealth.org914-493-3470

Backup ContactAbbas Smiley, MD

abbas.smiley@wmchealth.org914-493-3470

Outcome results

None listed

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