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Emergency General SurgerySTRATANCT07850401

STRATA: Surgical Treatment Using Robotic Approach in The Acute Abdomen

An observational study of Emergency General Surgery, run by Portsmouth Hospitals NHS Trust at 1 site in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Robotic surgery in the UK is now widely used in elective procedures based on evidence that it can improve outcomes, with improved vision and precision for the surgeon resulting in better results and greater rates of minimally invasive surgery. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Emergency General Surgery
How many people
600 participants
Where
1 siteUnited Kingdom
Study dates
24 Jul 2026to 20 Jul 2028
How long will I take part?
1 Year
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: WP1. Any patients who undergo emergency (non-elective) general surgery via any surgical approach, robotic, open or laparoscopic as determined by the treating physician. WP2. Patients presenting to hospital with emergency general surgery conditions.

Who may be able to join

  • Any patients who undergo emergency (non-elective) abdominal surgery
  • Patient scheduled to undergo either an open, robotic or laparoscopic approach to surgery
  • Willing and able to comply with study requirements
  • Must have access to an internet enabled device

Who cannot join

  • <18 years of age
  • Inability to give informed consent
  • Minor procedures: Appendicectomy, abscess drainage
  • Inability to return or complete electronic questionnaires
  • Mental incapacity to understand or consent to study procedures

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United Kingdom1 site, 1 recruiting
  • Portsmouth Hospitals University NHS Trust

    Portsmouth, Hampshire, PO6 3LY

    Research Office, 02392286000 ext. 5153, pho-tr.researchoffice-groupmailbox@nhs.net

    Recruiting

Other trials in United Kingdom

About this study

Robotic surgery in the UK is now widely used in elective procedures based on evidence that it can improve outcomes, with improved vision and precision for the surgeon resulting in better results and greater rates of minimally invasive surgery. Despite this, there remain some concerns about its use with some saying it adds cost with limited or no benefit to patients. Its application in the emergency setting has not been well studied. However, emergency patients are the sickest patients, and so stand to potentially gain the most from robotic surgery, if it is shown to be beneficial by enabling more precise surgery. The investigators aim to evaluate the impact of robotics in emergency general surgery, on outcomes, patients, and surgeons as well as the greater health system.

Given the need for modern health systems to reflect the needs and desires of their users, the investigators also aim to explore patient and surgeon preferences and priorities in emergency surgery with particular reference to surgical approach (open/laparoscopic/robotic).

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07850401
Study groupRoleWhat they receive
Patient Perspective GroupPatients presenting with emergency general surgery conditions.
Emergency Surgery GroupPatients undergoing emergency general surgery.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Post-operative complications reported

    Post-operative complications reported in health records and patient reported complications. Comparison of complications reported for robotics and non-robotic emergency surgery

    Measured: 1 year

Secondary outcomes (3)
  1. Pre-operative questionnaire

    Assessment of patient preferences and priorities in emergency surgery

    Measured: Pre-operative

  2. Local Experienced Discomfort Questionnaire

    Evaluation of surgeon related outcomes (ergonomics and discomfort) using the Local Experienced Discomfort Questionnaire

    Measured: Post-operation

  3. QoL15 and EQ5D-3L questionnaires

    Assessment of patient related clinical outcomes following robotic/laparoscopic emergency surgery i.e. QOL (pre-op and post-op) via QoR15 and EQ5D-3L questionnaires.

    Measured: up to 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Sep 2026
  2. Study start24 Jul 2026
  3. Primary completion20 Jul 2028 (estimated)
  4. Study completion20 Jul 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
600 participants (estimated)
Target duration
1 Year
IDs, dates and publications
ClinicalTrials.gov ID
NCT07850401
Sponsor's protocol ID
PortsmouthNHS
Acronym
STRATA
Status last verified
Sep 2026
First submitted
10 Jul 2026
Last updated
30 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Emergency General Surgery, run by Portsmouth Hospitals NHS Trust at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 30 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Post-operative complications reported (time frame: 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Sep 2026.

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