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The Influence of Blood Pressure Upon the Clarity of Surgical Field in Endonasal Surgery

The Influence of Blood Pressure Upon the Clarity of Surgical Field in Endonasal Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03815435
Enrollment
30
Registered
2019-01-24
Start date
2019-01-01
Completion date
2020-03-31
Last updated
2023-03-31

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

Conditions

Chronic Rhinosinusitis (Diagnosis)

Keywords

Surgical field clarity, Endonasal surgery, Intraoperative bleeding

Brief summary

The work compares the effect of different various values of arterial blood pressure on the clarity of the surgical field in pansinusoperation in patients with chronic rhinosinusitis.

Detailed description

The work compares the effect of different values of arterial pressure on the clarity of the surgical field in pansinus operation in patients with chronic rhinosinusitis. A secondary goal of the study is to compare circulatory parameters, depth of anaesthesia, near-infrared spectroscopy (NIRS) and consumption of hypotensives. Null hypothesis: There is no difference in the clarity of the surgical field at various levels of the mean arterial pressure. This study is being realized in accordance with the Declaration of Helsinki and has been approved by the Ethics Committee of the University Hospital Ostrava (849/2018). According to the statement of the State Institute for Drug Control of 26th April 2019 (reference number Sukl96964/2019), the trial is not considered a clinical trial of medicinal products. Study type: Single-blind study (the surgeon does not know the value of the patient's blood pressure) prospective study.

Interventions

PROCEDUREControlled hypotension

Controlled hypotension will be administered according to the clarity of the surgical field.

Sponsors

University Hospital Ostrava
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

The physician performing the surgery and assessing the surgical field clarity will be masked as to the value of the blood pressure in the individual patient.

Intervention model description

The study subjects will be enrolled into one arm.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with chronic rhinosinusitis undergoing pansinusoperation * Age over 18 years * Concrete surgeon (Petr Matoušek, MD, Ph.D., MBA) * Concrete anaesthetist (Michal Parma, MD)

Exclusion criteria

* Coagulopathy * Thrombocytopathies * Vascular wall disorders * Thrombophlebitis * Anticoagulation or anti-aggregation therapy * History of malignancy * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Surgical field clarity in relation to the value of arterial pressure13 monthsClarity of the surgical field will be assessed on a scale of 0-5, according to the Boezaart's system (1995)

Secondary

MeasureTime frameDescription
Blood pressure13 monthsBlood pressure will be measured in the morning before surgery, on arrival at the operating theatre and further 5 minutes after anaesthesia, and every five minutes during the surgery.
Heart rate13 monthsHeart rate will be measured in the morning before surgery, on arrival at the operating theatre and further 5 minutes after anaesthesia, and every five minutes during the surgery.
Depth of anaesthesia13 monthsDepth of anaesthesia will be measured using the BIS value every 5 minutes
Near infrared spectroscopy (NIRS)13 monthsCerebral perfusion will be measured using the NIRS value every 5 minutes
Consumption of hypotensives13 monthsConsumption of hypotensives (Nitro Pohl) will be measured in mg/hr
Blood loss13 monthsBlood loss (ml) during the surgery will be measured
Recovery from anaesthesia duration13 monthsThe interval from the end of surgery to eye opening in minutes will be measured.
Postoperative pain13 monthsPostoperative pain will be measured using the VAS (Visual Analogue Scale) upon arrival to the recovery room and the standard ward.
Cognitive function13 monthsThe standardised clock-drawing test will be performed at the ward, 2 hours after surgery.
Postoperative nausea13 monthsThe presence of postoperative nausea (YES/NO) will be observed.
Postoperative vomiting13 monthsThe presence of postoperative vomiting (YES/NO) will be observed.
Complications of controlled hypotension13 monthsThe presence of complications of controlled hypotension (stroke, myocardial infarction, kidney injury - YES/NO) will be observed.
Use of tamponade13 monthsThe need to use tamponade due to bleeding (YES/NO) will be observed.
Surgical revision13 monthsThe need for surgical revision due to bleeding (YES/NO) will be observed.

Countries

Czechia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026