- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06036641
The Effects of Prolonged Head-Down Tilt Lithotomy Position on Lower Limb Haemodynamics (HELP)
The Effects of Prolonged Head-Down Tilt Lithotomy Position on Lower Limb Haemodynamics in Adults Undergoing Minimally Invasive Abdominopelvic Surgery: An Intraoperative Observational Study
Study Overview
Status
Intervention / Treatment
Detailed Description
The development of lower limb compartment syndrome in the absence of trauma (known as well-leg compartment syndrome, WLCS) is a severe complication reported during prolonged pelvic surgery. WLCS is characterised by muscular ischaemia and secondary necrosis from the increase in hydrostatic pressure in a closed fascial compartment.
The aetiology of WLCS appears to be primarily related to ischaemia of the lower limbs after a prolonged period in the head-down tilt lithotomy (HDTL) position, which is commonly used to access the pelvis and perineum during urological, colorectal, and gynaecological surgery. Elevation of the lower limbs above the heart results in a ~2 mmHg drop in mean arterial pressure at the mid-calf for every 2.5 cm that the limbs are raised. These hemodynamic changes are accompanied by an increase in compartment pressures associated with limb elevation and are further exacerbated by a steep (>15°) head-down tilt. The outcome of these changes ultimately leads to the development of significant and (often unrecognised) intraoperative ischemia in the lower limbs.
Prolonged reductions in lower limb perfusion during HDTL can cause the development of localised tissue oedema, leading to marked intracompartmental hypertension, which is further exacerbated once the limbs are lowered and reperfusion of ischemic muscle occurs. This is a consequence known as ischaemic-reperfusion injury (IRI), a phenomenon where reperfusion per se may result in a local and systemic inflammatory response that may augment tissue injury in excess of that produced by ischaemia alone.
Microvascular injury is considered one of the major determinants of IRI, particularly due to increased permeability of capillaries and arterioles that lead to an increase in diffusion and fluid filtration across the tissues. Subsequently, activated endothelial cells produce more reactive oxygen species and less nitric oxide, and this imbalance results in a corresponding inflammatory response and increased oxidative stress, which if sufficiently severe lead to further lower limb muscle and nerve injury.
The incidence of WLCS is unpredictable and as the individual is anaesthetised, the diagnosis is delayed in many cases, so the residual motor-sensory deficit may be severe, even after fasciotomy. Although there are many published case reports of this condition, it is likely that many cases of WLCS go unreported, and some may be mild and escape clinical detection. However, in cases that have been reported, the incidence of permanent disability after the development of WLCS ranges from ≈30% to ≈100%.
The paucity of detailed observational studies into the effects of HDTL on lower limb haemodynamics and tissue oxygenation has restricted the ability of the clinical and scientific society to construct clinical strategies to minimise this complication. Identifying individuals with risk factors and increasing surveillance during surgery in these people may allow for early detection and decrease the morbidity and potential mortality associated with intraoperative WLCS.
The study aims to assess lower limb haemodynamics by measuring cutaneous blood flow, muscle and brain tissue oxygenation, inflammatory and oxidative stress biomarkers during pelvic surgery in patients placed in HDTL. This study has the potential to provide a better understanding of the pathogenesis of WLCS and add novel knowledge regarding its early diagnosis.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
West Sussex
-
Portsmouth, West Sussex, United Kingdom, PO6 3LY
- Queen Alexandra Hospital, Portsmouth Hospitals University NHS Trust
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults scheduled to undergo colorectal surgery in the HDTL position
Exclusion Criteria:
- History of myocardial infarction or cerebro-vascular events in the last 12 months
- Previous revascularisation procedure in their lower limbs
- BMI > 40 kg/m2
- Inability to give informed consent
- Other serious medical conditions, which in the opinion of study investigators, would interfere with safety or data interpretation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Colorectal surgery
Individuals scheduled for colorectal surgery in the HDTL position
|
All participants will undergo NIRS monitoring of muscle and cerebral tissue oxygenation intraoperatively.
Cutaneous blood flow will be assessed intraoperatively via Laser Doppler flowmetry in all participants
Blood samples will be taken to measure biomarkers of inflammation and oxidative stress at specific time points
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cutaneous blood flow
Time Frame: baseline, during the surgery
|
Change over time in cutaneous blood flow in the legs relative to a vascular occlusion test (VOT) during surgery in the HDTL position.
|
baseline, during the surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle tissue oxygenation
Time Frame: baseline, during the surgery
|
Change over time in muscle tissue oxygenation in the lower limb relative to a vascular occlusion test (VOT) during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Plasma interleukin-6 (IL-6) concentration
Time Frame: baseline, during the surgery
|
Change over time in [IL-6] during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Plasma Tumour Necrosis Factor Alpha (TNF-α) concentration
Time Frame: baseline, during the surgery
|
Change over time in [TNF-α] during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Plasma Superoxide Dismutase (SOD) concentration
Time Frame: baseline, during the surgery
|
Change over time in [SOD] during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Plasma Protein Carbonyl concentration
Time Frame: baseline, during the surgery
|
Change over time in [protein carbonyl] during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Plasma nitrate concentration
Time Frame: baseline, during the surgery
|
Change over time in [nitrate] during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Plasma nitrite concentration
Time Frame: baseline, during the surgery
|
Change over time in [nitrite] during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Mean arterial pressure (MAP)
Time Frame: baseline, during the surgery
|
Change over time in MAP during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Skin temperature
Time Frame: baseline, during the surgery
|
Change over time in skin temperature during surgery in the HDTL position.
|
baseline, during the surgery
|
|
Brain tissue oxygenation
Time Frame: continuous measurement during the surgery
|
Change over time in brain tissue oxygenation during surgery in the HDTL position.
|
continuous measurement during the surgery
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Chukwuemeka C Uzoma, MBBS, University of Portsmouth
- Principal Investigator: Maria C Perissiou, PhD, University of Portsmouth
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRAS [287464]
- CPMS ID - 56254 (Other Identifier: NIHR Clinical Research Network (NIHR CRN))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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