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Anastomotic LeakCALMNCT05000580

Colorectal Anastomotic Leak Management

An observational study of Anastomotic Leak, run by Surgical Trainees East of England Research Collaborative at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Colorectal anastomotic leaks (AL) are associated with high morbidity and mortality. Management of AL and its intra-operative decision making is often difficult. The aim of this multi-centre study is to explore different management strategies, including different surgical options, and analyse rates and patterns of… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Anastomotic Leak
What is being tested?
Surgical
Type of treatment
Surgery or procedure
How many people
201 participants
Where
1 siteUnited Kingdom
Study dates
1 Jan 2020to 1 Jul 2021
Phase
Observational
Are there results?
None posted in the registry

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
  • Adult, Older adult

Study population: Patients can be identified and recruited to the study through a variety of ways: * Multi-Disciplinary Teams (MDTs): Most MDTs will record data as to who has had a leak and what treatment they have had or are to have * Colorectal Clinical Nurse Specialists (CNS): In most trusts, the CNS keep records of patients who have had complications * National Bowel Cancer Audit (NBOCAP): Although this will not capture patients who have had benign disease, it will provide data on patients with cancer * Consultants: Many consultants collect their own data, and this can be an excellent source of information

Who may be able to join

  • Age ≥18 years old
  • Patients undergoing colorectal anastomosis for any pathology (benign or malignant), during an elective or emergency admission, who had an AL.
  • Laparoscopic or open surgery

Who cannot join

  • IBD, Small bowel anastomosis,

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Watford General Hospital

    Watford, WD18 0HB

Other trials in United Kingdom

About this study

Official title: Management of Anastomotic Leaks After Elective Colorectal Resections: The East of England Experience - A Retrospective Cohort

Colorectal anastomotic leaks (AL) are associated with high morbidity and mortality. Management of AL and its intra-operative decision making is often difficult. The aim of this multi-centre study is to explore different management strategies, including different surgical options, and analyse rates and patterns of failure of initial management.

All consecutive patients who had a confirmed AL after elective colorectal resections from 1st January 2014 to 31st December 2019 were included at seven hospitals across the East of England Region. Morbidity (length of stay, and failures) and mortality were compared across the different management strategies, and survival analyses were performed.

Read the detailed description

The International Study Group of Rectal Cancer proposed a grading system for the management of colorectal anastomotic leaks (Rahbari et al., 2010). Grade A anastomotic leaks are identified by radiographic findings of a perianastomotic fluid collection, leakage of contrast through the anastomosis, or observation of new drainage of enteric contents through either a drain or through a fistula but without accompanying clinical complaints. These may be managed expectantly. These may become apparent during the preoperative work-up prior to closure of a diverting ostomy and will at least delay reversal. Grade B leakage requires therapeutic intervention but does not necessarily require reoperation. Antibiotics and percutaneous drainage of fluid collections are the most common nonoperative interventions. Grade C anastomotic leakage requires relaparotomy. Surgical treatment is performed with the goal of controlling life-threatening sepsis. The traditional operation with takedown of the anastomosis and end colostomy may be appropriate, but washout with drain placement and diverting loop ileostomy may also be appropriate. 1 Elective colorectal resection surgeries have an over 30-day mortality rate of 5.8%. While emergency resections have a 7.8% mortality (Morris, 2011). Experiencing an anastomotic leaks should not have a higher mortality than the above rates.

Aim The main interest of this study is to firstly assess our practice and management of AL, evaluate whether hospitals in the region are identifying AL as per The International Study Group of Rectal Cancer, grading the AL as Grade A, B, and C above, and analyse the natural evolution of leaks and their subsequent treatment(s).

Outcomes of Interest

Management of anastomotic leaks and associated outcome in terms of:

Primary objectives:

  1. 2-year mortality after anastomotic leaks of different grades. Standards of reference for audit: Elective colorectal resection surgeries have an over 30-day mortality rate of 5.8%. While emergency resections have a 7.8% mortality (Morris, 2011). Experiencing an anastomotic leaks should not have a higher mortality than the above rates.
  2. Outcomes of different treatment strategies of Colorectal anastomotic leaks.
  3. Grading of AL as described above.

Secondary Objectives include:

  • Need for subsequent management strategies after failure of initial strategy.
  • Proportion requiring laparotomy, bowel resection, defunctioning.
  • Length of ITU stay, overall length of hospital stay
  • Non-surgical complications (pneumonia, urine infection, DVT, PE, MI etc)
  • Delay / change in oncological management Methods Data will be collected retrospectively going back to 2014 (five years), at multiple East of England sites. The study will initially commence across trusts in the East of England Deanery however efforts will be made to recruit other research collaboratives through existing and established ties with the National Research Collaborative.

Population Identification

Patients can be identified and recruited to the study through a variety of ways:

  • Multi-Disciplinary Teams (MDTs): Most MDTs will record data as to who has had a leak and what treatment they have had or are to have
  • Colorectal Clinical Nurse Specialists (CNS): In most trusts, the CNS keep records of patients who have had complications
  • National Bowel Cancer Audit (NBOCAP): Although this will not capture patients who have had benign disease, it will provide data on patients with cancer
  • Consultants: Many consultants collect their own data, and this can be an excellent source of information An estimated of 10-30 leaks occur every year at each site. We expect to have between 30-60 leaks with 3 year follow up per hospital site.

Study duration Data collection 3-6 months from date of project launch (October 2019). Reminders for date of study closure will be sent closer to the time.

Variables

It must be stated that the aim of this study is not to investigate 'leak-rates' or comparatively analyse data of individual surgeons or trusts. No patient identifiable or surgeon identifiable information will be requested. Data and outcomes from individual trusts will not be compared against each other. The name of the trust will be recorded as one of the variables only for data validation purposes and to identify the lead investigators at each trust for the purposes of communication only. Names of Trusts or Surgeon level details will not be published. The variables that will be recorded are as follows:

  • Trust
  • Local Patient ID
  • Gender (M/F)
  • Age At Time (of Surgery) (Whole number)
  • Indication for surgery (where is cancer, IBD?)
  • Comorbidity 1 (in any order)
  • Comorbidity 2 (in any order)
  • Comorbidity 3 (in any order)
  • Comorbidity 4 (in any order)
  • Date of Index Surgery
  • Type of Index Surgery (right, left, segmental sigmoid colectomy, AR)
  • Elective / emergency
  • Date Leak Detected
  • Leak size (description on CT (size, localized, small, free)
  • Symptomatic/Non-Symptomatic Leak
  • Treatment 1 (IV antibiotics are always given once a leak is diagnosed. So it should not be inserted automatically as treatment 1. So I would reserve inserting "IV antibiotics" or "conservative" as treatment 1 unless the patients actually had a trial of conservative management.)
  • date treatment 1 (chronological order)
  • Treatment 2
  • date treatment 2 (chronological order)
  • Treatment 3
  • Date treatment 3 (chronological order)
  • Type of Rescue Surgery Performed (?laparotomy, bowel resection, defunctioning)
  • Length of Stay in ITU Post Leak (in days)
  • Length of stay in Leak episode (total in days, if the leak occurred during the index operation episode, it is the total length of stay in that whole episode.)
  • Date CT confirmed leak resolved
  • Number of days of drainage (if drain inserted. This column is for radiologically inserted drains; or EUA inserted drains in low pelvic leaks. It is the total number of days a drain was kept in until removal of the drain (including changes).)
  • Date of Death
  • Date last seen alive (censored)
  • Other Comments

Inclusion:

  • Age ≥18 years old
  • Patients undergoing colorectal anastomosis for any pathology (benign or malignant), during an elective or emergency admission, who had an AL.
  • Laparoscopic or open surgery Ethical approval \& Registrations This is a retrospective audit, aiming to analyse the region trust's management of colorectal anastomotic leaks, and whether this is in accordance with published literature. This study therefore needs to be registered as a retrospective audit in each trust. Please keep a record of those that were subsequently excluded and the reason why (most probably was not a leak, or not managed as leak).
Being tested
Surgical
Medical subject headings
Anastomotic Leak

What participants receive

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

  • SurgicalProcedure or surgery

    Conservative vs surgical management

What is being measured

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

  1. failure rate of initial management strategy

    failure rate of initial management strategy

    Measured: 5 years

Secondary outcomes (2)
  1. mortality

    Kaplan-Meier Survival curve

    Measured: 5 years

  2. length of stay

    in days

    Measured: 5 years

Timeline

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

  1. First posted11 Aug 2021
  2. Study start1 Jan 2020
  3. Primary completion1 Jun 2021
  4. Study completion1 Jul 2021

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
Retrospective
Enrolment
201 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05000580
Sponsor's protocol ID
CALM-V3
Acronym
CALM
Status last verified
Aug 2021
First submitted
29 Jul 2021
Last updated
11 Aug 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Aker M, Askari A, Rabie M, Aly M, Adegbola S, Patel K, Currow C, Nunn R, Hadjittofi C, Rankin A, Halai S, Elsamani K, Bondje S, Mohamed I, Lee J, Wong J, Robertson-Waters E, Uddin A, Hollingshead J. Management of anastomotic leaks after elective colorectal resections: The East of England experience. A retrospective cohort. Int J Surg. 2021 Dec;96:106167. doi: 10.1016/j.ijsu.2021.106167. Epub 2021 Nov 6.

    PubMed 34752951

Questions about this trial

What is this clinical trial studying?

An observational study of Anastomotic Leak, run by Surgical Trainees East of England Research Collaborative 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 3 inclusion and 1 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: finished, as of the sponsor's last update on 11 Aug 2021. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

failure rate of initial management strategy (time frame: 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05000580, which also lists 1 linked publication.

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 11 Aug 2021.

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