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The Effects of Preloading Before Beach Chair Position

Effectiveness of Preloading Before Beach Chair Position on Patients Undergoing Arthroscopic Shoulder Surgery: Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04671537
Enrollment
49
Registered
2020-12-17
Start date
2018-06-01
Completion date
2020-01-01
Last updated
2020-12-17

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

Conditions

Anesthesia, Hemodynamic Instability, Shoulder Injuries

Keywords

beach chair position, arthroscopic shoulder surgery, preloading, hemodynamic stability, postoperative nausea and vomiting

Brief summary

The main objective of this study is whether preloading before positioning would be effective for less hemodynamic instability. The study also analyzes that patients with preloading will decrease postoperative nausea and vomiting, better surgical satisfaction and shortened the duration of surgery and anesthesia.

Detailed description

Keeping patients in normovolemic state and hemodynamically stable in anesthesia and intensive care practice are important goals of anesthesiologist. It is known that hypotension that develops after taking patients to the beach chair position has a negative effect on cerebral oxygenation. Aggressive fluid regimes using to prevent hypotension can cause glycocalyx damage, edema and organ dysfunction. Also hypertension seconday to vasopressor therapy can cause bleeding at the surgical site and impaired surgical visualization during the arthroscopic shoulder surgery. In the literature, there are studies examine whether the hypotension is the result of decreased cardiac output or decreased systemic resistance and what should be the optimal treatment , but as far as investigators know, there is no study about effects of preloading before the beach chair position on hemodynamic parameters.

Interventions

DRUGPreloading with crystalloid fluid

crystalloid fluid at 10 ml/kg of ideal body weight was administered intravenously in 30 min before the BCP for patients

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Single-blind

Intervention model description

Study group - Control group

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* undergoing elective arthroscopic shoulder surgery in the BCP, * age older than 18 years and younger than 65 years, * the American Society of Anesthesiologist (ASA) physical status of I or II, * accepting the study protocol.

Exclusion criteria

* preoperative arrhythmia, * significant heart failure * valvular heart disease, * preexisting cerebrovascular disease, * deciding to switch to open surgery, * vasopressor infusion during the surgery, * using angiotensin converting enzyme inhibitors (ACEI) orangiotensin receptor blockers (ARB) as antihypertensive medication.

Design outcomes

Primary

MeasureTime frameDescription
Mean arterial pressureduring surgery (spesicific time intervals (after induction - after BCP position - 0th min - 5th min - 10th min- 30th min- 60th min)(mmHg)
Cardiac outputduring surgery (spesicific time intervals (after induction - after BCP position - 0th min - 5th min - 10th min- 30th min- 60th min)(L/min)
Stroke volume variationduring surgery (spesicific time intervals (after induction - after BCP position - 0th min - 5th min - 10th min- 30th min- 60th min)(%) data obtained from arterial contour analysis
Heart rateduring surgery (spesicific time intervals (after induction - after BCP position - 0th min - 5th min - 10th min- 30th min- 60th min)bpm

Secondary

MeasureTime frameDescription
Postoperative nausea and vomitingin postoperative first dayPONV rates
Total amount of crystalloid and colloidduring surgeryTotal amount of crystalloid and colloid (ml)
Surgical satisfaction ratein postoperative first daySurgical satisfaction scale (0-10, 0 lowest score, 10 highest score) (score)
The duration of anesthesia and surgeryduring surgeryThe duration of anesthesia and surgery (min)
Ephedrine usageduring surgerytotal ephedrine dose (mg) used during surgery

Countries

Turkey (Türkiye)

Outcome results

None listed

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