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Effects of Preoperative Anxiety and Pain Sensitivity in Cases of Endoscopic Ultrasonography Received Sedoanalgesia

The Effects of Preoperative Anxiety and Pain Sensitivity on the Intraoperative Hemodynamics, Consumption of Propofol and Postoperative Recovery in Cases of Endoscopic Ultrasonography (EUS) Received Sedoanalgesia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03114735
Enrollment
80
Registered
2017-04-14
Start date
2017-04-15
Completion date
2017-06-01
Last updated
2017-04-14

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

Conditions

Sedoanalgesia

Brief summary

The objective of this study was to detect whether preoperative anxiety and pain sensitivity had effects on the consumption of anesthetics, time to achieve desired level of sedation, patient and endoscopist satisfaction, and postoperative recovery time and pain in deep sedation.

Interventions

None listed

Sponsors

Istanbul Medeniyet University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years

Inclusion criteria

* ASA 1-2 category * between the ages of 20 and 65 * patients who has an education level and mental state to complete the scale and questionnaire provided for assessment

Exclusion criteria

* patients who has a psychiatric and neurological disease and use psychiatric drugs and chronic alcohol intake

Design outcomes

Primary

MeasureTime frameDescription
consumption of propofol(mg)1-3 hoursinitial dose infusion of 1 mg.kg-1 , maintenance dose 2 mg/kg/h, additional dose 0,1mg/kg in case of insufficient sedation
the heart rate(n/min)1-3 hoursDuring procedure
arterial pressure(mmHg)1-3 hoursDuring procedure
peripheral oxygen saturation(%)1-3 hoursduring procedure
postoperative nausea and vomiting (Numeric Rank Score)1-3 hoursAfter procedure
Post-procedure pain(Visual Analog Score)1-3 hoursAfter procedure

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026