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OpenTrials
Completed

NCT Number: NCT07047911

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

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Observational only - surgical management not assigned by study

Other

Observational only - surgical management not assigned by study

Primary outcomes

  1. Post operative morbidity

    Time frame: 30days

  2. Post operative morbidity

    Time frame: 30 days

Sponsors and collaborators

Lead sponsor

Government Medical College, Patiala

Other Gov

Registry information

Acronym: PERIMOPP

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Jul 2, 2025
Registry last updated
Jul 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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