New guidelines aim to cut hospital stays for acute abdomen in zambia
NCT ID NCT07587190
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether new practice guidelines for acute abdomen (sudden severe stomach pain) can help doctors in Zambia's primary care clinics manage patients better. Researchers will compare hospital stay lengths between a clinic using the guidelines and one that does not. The goal is to see if the guidelines reduce time in the hospital and improve care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- practice guidelines for acute abdomen
- What this could lead to
- If successful, this could lead to better management of acute abdomen in low-resource settings, potentially reducing hospital stays and deaths.
- What could go wrong
- This is an early-stage implementation study with no direct treatment. Results may not apply to other settings, and the guidelines may not improve outcomes as hoped.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 280 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Data from all patients 18 year and older with acute abdomen including surgical, gynecological and medical acute abdomen managed at the intervention site and control site will be collected during the study period. Exclusion Criteria: * All cases of acute abdomen secondary to trauma will be excluded from the study. All patients in the immediate postoperative phase operated from other facilities presenting with acute abdomen.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Kanyama First Level Hospital and Matero First Level Hospital
RECRUITINGLusaka, Lusaka Province, 10101, Zambia