NCT05623176 Clinical Outcomes and Equality in Healthcare for Emergency General Surgery Patients Undergoing Emergency Laparotomy
| NCT ID | NCT05623176 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Region Stockholm |
| Condition | Abdomen, Acute |
| Study Type | OBSERVATIONAL |
| Enrollment | 2,000 participants |
| Start Date | 2015-01-01 |
| Primary Completion | 2030-12 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 2,000 participants in total. It began in 2015-01-01 with a primary completion date of 2030-12.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this observational cohort study is to evaluate the standard of care for general surgerical patients undergoing emergency laparotomy and assess factors affecting clinical outcomes, as well as evaluating the quality of life in the year after abdominal surgery. The main questions it aims to answer are: 1. what factors are associated with adverse post-operative events 2. are patients treated differently based on sex or age 3. how does quality of life look like and possibly change over the coarse of a year after surgery This is an evaluation of the current standard of care and the outcomes of this patient group prior to the implementation of a standardised care protocols for emergency laparotomy patients. Secondly, the study aims to, over time, compare results before and after the introduction of this standardised care protocol.
Eligibility Criteria
Inclusion Criteria: * Undergoing emergency laparotomy due to general surgical indication Exclusion Criteria: * Children under 16 * Trauma laparotomy * Vascular, urological or gynaecological indication for laparotomy
Contact & Investigator
Rebecka Ahl Hulme, MD PhD
PRINCIPAL INVESTIGATOR
Karolinska University Hospital
Frequently Asked Questions
Who can join the NCT05623176 clinical trial?
This trial is open to participants of all sexes, aged 16 Years or older, studying Abdomen, Acute. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05623176 currently recruiting?
Yes, NCT05623176 is actively recruiting participants. Contact the research team at rebecka.ahl-hulme@regionstockholm.se for enrollment information.
Where is the NCT05623176 trial being conducted?
This trial is being conducted at Stockholm, Sweden.
Who is sponsoring the NCT05623176 clinical trial?
NCT05623176 is sponsored by Region Stockholm. The principal investigator is Rebecka Ahl Hulme, MD PhD at Karolinska University Hospital. The trial plans to enroll 2,000 participants.