Impact of Nutritional Deficit in Emergency Surgery

NCT ID: NCT04696367

Last Updated: 2021-10-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

59 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-01

Study Completion Date

2021-05-30

Brief Summary

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Patients in emergency settings might become malnourished. There are different ways to identify the group as 'at risk' of malnutrition. There are also several different ways to measure outcomes. This pilot study will look at patients undergoing emergency laparotomy, investigate relationships between different selection criteria and outcome measures, and test feasibility of outcome measure collection.

Detailed Description

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Patients in emergency settings might become malnourished. There are different ways to identify the group as 'at risk' of malnutrition. There are also several different ways to measure outcomes. This pilot study will look at patients undergoing emergency laparotomy, investigate relationships between different selection criteria and outcome measures, and test feasibility of outcome measure collection.

Conditions

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Emergencies Surgery Malnutrition

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with acute intra-abdominal pathology

Patients admitted to hospital with acute intra-abdominal pathology

Emergency laparotomy

Intervention Type PROCEDURE

Midline laparotomy for acute intra-abdominal pathology

Interventions

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Emergency laparotomy

Midline laparotomy for acute intra-abdominal pathology

Intervention Type PROCEDURE

Other Intervention Names

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Celiotomy

Eligibility Criteria

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Inclusion Criteria

* Willing to consent,

-≥ 18 years old
* eligible for inclusion in National Emergency Laparotomy Audit
* first procedure during admission (\<7 days from admission).

Exclusion Criteria

* Recent discharge from hospital (within 60 days),
* unable to provide informed consent
* life expectancy \<12 months
* prisoners
* lack mental capacity
* language barrier affecting ability to provide consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sheffield Teaching Hospitals NHS Foundation Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Timothy O'Connor, MBChB

Role: PRINCIPAL_INVESTIGATOR

Sheffield Teaching Hospitals NHS Foundation Trust

Locations

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Doncaster Royal Infirmary

Doncaster, South Yorkshire, United Kingdom

Site Status

Sheffield Teaching Hospitals

Sheffield, South Yorkshire, United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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STH20936

Identifier Type: -

Identifier Source: org_study_id

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