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Investigating the impact of surgical operations on the human immune system

Investigating the immune response in patients undergoing surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN13131952
Enrollment
40
Registered
2024-10-16
Start date
2025-05-26
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients undergoing elective surgery Surgery

Interventions

Two blood samples will be taken from elective surgery patients
one before surgery and the second following the completion of the operation. Blood samples will be subjected to laboratory analysis examining the immune and inflammatory response to the surgical inter

Sponsors

University of Birmingham
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male or female patients aged 18-65 years 2. Patient able to give informed consent 3. Patient undergoing elective open abdominal wall reconstruction surgery

Exclusion criteria

Exclusion criteria: 1. Under the age of 18 years and over the age of 65 years 2. A known malignancy 3. Pregnancy 4. The operation is contaminated (e.g. there is a bowel resection +/- anastomosis, iatrogenic bowel injury or presence of a stoma) 5. Minimally invasive (laparoscopic or robotic) surgery 6. Significant anaesthetic complication (such as anaphylaxis, malignant hyperthermia, negative pressure pulmonary oedema)

Design outcomes

Primary

MeasureTime frame
The metabolic activity of neutrophils and monocytes isolated from blood samples obtained from elective surgery patients will be measured by flow cytometry, enzyme-linked immunosorbent assays and metabolic tracing before and after their operation

Secondary

MeasureTime frame
The following secondary outcome measures will be assessed in blood samples obtained from elective surgery patients before and after their operations: 1. Anti-microbial activities and surface phenotype of isolated neutrophils, monocytes and/or peripheral blood mononuclear cells (in the absence and/or presence of ex vivo stimulation) will be measured using flow cytometry 2. Circulating markers of inflammation (e.g. pro-inflammatory cytokines, acute phase proteins, cell-free DNA, Damage-associated molecular patterns, whole blood cell counts) will be measured using enzyme-linked immunosorbent assays, whole blood cell haematological analysers and fluorometric-based assays 3. DNA and RNA epigenetic profiles of neutrophils and peripheral blood mononuclear cells RNA sequencing, DNA methylation assays and real-time polymerase chain reaction (RT-PCR) experiments

Countries

England, United Kingdom

Contacts

Public ContactJon Hazeldine
j.hazeldine@bham.ac.uk+44 (0)121 371 3264

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026