N/A N=91

Descriptive and Correlational Study of Peritonitis in Haiti.

Peritonitis

Bottom Line

View on ClinicalTrials.gov: NCT04182217 ↗

Enrolled (actual)

Serious AEs

23.1%

Results posted

Feb 2020

Primary outcome: Primary: Heart Rate — 108.18 Beats/min

Study Design & Population

Study type: Observational
Phase: N/A
Interventions: Epidemiological description (Other)
Age: Pediatric, Adult, Older Adult · 11+ yrs
Sex: All
Sponsor: Universite d'Etat d'Haiti
Primary completion: Mar 2019

Outcome Measures

Outcome	Result	p-value
PRIMARY Heart Rate	108.18	—
PRIMARY Respiratory Rate	28.58	—
PRIMARY Temperature	37.52	—
PRIMARY Blood Pressure	110.93	—
PRIMARY Etiological Diagnosis	—	—
PRIMARY Demographic Parameters	—	—
SECONDARY Onset of Symptoms	6.9	—
SECONDARY Delay in Pre-op	3.73	—
SECONDARY Delay in Post-op	9.19	—
SECONDARY Delay in Hospital	12.82	—

Summary

The primary objective: To study the prevalence, etiology, and factors associated with the severity of peritonitis and its complications in the surgery department of the State University Hospital of Haiti. Secondary objectives: * Identify epidemiological characteristics. * Describe the main etiologies encountered in the service * Measure the time required for treatment and its consequences on the evolution of peritonitis.

Eligibility Criteria

Inclusion Criteria

Patients whose peritonitis diagnosis was made and operated on in the department during the period.

Patient whose record is identified (with age, sex) with at least the clinical and etiological diagnosis identified in the operating protocol.

Exclusion Criteria

Patients with incomplete records.

Cases of post-operative peritonitis.

Patient under 10 years of age

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04182217). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.