NCT05230264

Brief Summary

It is recognised that women are at greater risk of death, complications and longer hospital stay following intact abdominal aortic aneurysm (AAA) repair, and the reason for this is not yet established. This disparity in outcomes for women compared to men is also recognised in other forms of cardiovascular surgery, which raises the question of whether women and men are reacting differently to the stress of operative repair. This study aims to examine whether there are differences baseline stress markers and in the stress response to AAA repair between men and women. It will also examine whether markers of stress are associated with poor clinical outcomes and slower recovery (indicated by longer hospital stay). The study will take the form of an observational cohort study. It will not alter any of the treatment that men and women receive, but will monitor their stress levels using physiological markers (through ECG (electrocardiogram) monitoring using a non-invasive holter, biochemical markers using blood samples (which will be taken at the same time as routine testing, so as not to require further invasive procedures), and psychological testing, using short forms that the patient will be able to fill out independently at different stages of their recovery. Clinical data will be used to look for relevant factors (clinical history or medications) which may alter the stress markers we are observing, and to compare outcomes with markers of stress. Patients will be asked for their consent to share their data with the research team in order to participate in the study. It will be made clear that there will be no change in their clinical or operative management if they participate in the study and they will be able to withdraw consent for further participation at any time.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2022

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 18, 2022

Completed
14 days until next milestone

Study Start

First participant enrolled

February 1, 2022

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 8, 2022

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2023

Completed
Last Updated

February 8, 2022

Status Verified

January 1, 2022

Enrollment Period

1.7 years

First QC Date

January 18, 2022

Last Update Submit

January 28, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • Biochemical measures of stress: level of serum cortisol & dehydroepiandrosterone (DHEA)

    Sex-specific differences in baseline and timing/magnitude of response to operative stress.

    Samples taken on the morning of operation (baseline), at anaesthetic induction, at the end of the procedure, 6 hours post-procedure and early morning samples during the remaining inpatient stay.

Secondary Outcomes (2)

  • Physiological parameters: assessment of beat-to-beat heart rate variability metrics.

    Baseline recording compared to post-operative recording of patient recovery during inpatient stay.

  • Psychological measures of stress: measured by State Trait Anxiety Inventory-Y and self assessment (Likert Scale).

    Pre-operative assessment compared to post-operative assessment at specified intervals during operative recovery - 2, 14, 30 and 90 days post-operation.

Study Arms (2)

Men

Elective AAA Repair

Other: Elective AAA Repair

Women

Elective AAA Repair

Other: Elective AAA Repair

Interventions

Elective AAA Repair - Observation of Stress Response

MenWomen

Eligibility Criteria

Age50 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Men and women undergoing primary elective intact AAA repair, open or endovascular (EVAR) at participating centres. Consecutive recruitment.

You may qualify if:

  • Men and women undergoing primary elective intact AAA repair, open or endovascular (EVAR) at participating centres.
  • Capacity to consent.

You may not qualify if:

  • Participants undergoing a secondary or emergency aortic procedure, or procedure for alternative aortic pathology.
  • Relevant confounding pathology such as hypothalamic-pituitary axis pathology (e.g. Addison's disease).
  • Lack of capacity to consent.
  • Participants with pacemaker dependency, or a significant arrhythmia, will be excluded from analysis of heart rate variability, but will be included in the study for analysis of psychological and biochemical markers of stress.
  • Participants on steroid treatment will also be excluded from analysis of biochemical markers but may be included for analysis of physiological markers and/or heart rate variability.
  • Participants must be over the age of 50 (In order to facilitate capture of degenerative aortic aneurysmal pathology rather than an alternative aortic pathology e.g. traumatic, connective tissue disorder).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Imperial College London

London, United Kingdom

Location

MeSH Terms

Conditions

Aortic Aneurysm, Abdominal

Condition Hierarchy (Ancestors)

Aortic AneurysmAneurysmVascular DiseasesCardiovascular DiseasesAortic Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 18, 2022

First Posted

February 8, 2022

Study Start

February 1, 2022

Primary Completion

October 1, 2023

Study Completion

October 1, 2023

Last Updated

February 8, 2022

Record last verified: 2022-01

Locations