Predictors of Morbidity in Perforation Peritonitis: A Prospective Observational Study From a Tertiary Care Centre in North India

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07047911

Acronym

PERIMOPP

Enrollment

Registered

2025-07-02

Start date

2014-03-10

Completion date

2016-05-10

Last updated

2025-07-02

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

Conditions

Peritonitis Infectious, Gastrointestinal Perforation, Surgical Infection, Postoperative Complications

Brief summary

This is a prospective observational cohort study conducted at a tertiary care hospital in North India. The study aims to evaluate clinical and biochemical predictors of postoperative morbidity in patients undergoing emergency laparotomy for gastrointestinal perforation peritonitis. Data on patient demographics, comorbidities, surgical timing, renal function, and complications were collected and analyzed to identify factors associated with increased morbidity. The findings are expected to support early risk stratification and improved clinical management of surgical emergencies.

Interventions

OTHERObservational only - surgical management not assigned by study

Observational only - surgical management not assigned by study

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Adults (\>18 years) with gastrointestinal perforation-induced peritonitis

Exclusion criteria

* Primary peritonitis, anastomotic leaks, refusal of surgery, or patients discharged against medical advice

Design outcomes

Primary

Measure	Time frame
Post operative morbidity	30days

Outcome results

None listed

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