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NCT03958578 Clinical Trial

The Effect of Preoperative Anxiety on Duration and Efficacy of Motor and Sensory Block in Spinal Anesthesia

Anxiety Clinical Trial

Official title:
The Effect of Preoperative Anxiety on Duration and Efficacy of Motor and Sensory Block in Spinal Anesthesia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03958578
Other study ID # OKMEYDANI EAH 48670771-514.10
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2019
Est. completion date December 1, 2019

Study information
Verified date November 2021
Source Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Spinal anaesthesia results in blockade of sympathetic efferent neurones. Patients with higher baseline sympathetic activation have been shown to have more marked hypotension after spinal anaesthesia. Anxiety causes generalized sympathetic activation. It was aimed to find the effect of preoperative anxiety on the duration and efficacy of neuraxial anaesthesia.

Recruitment information / eligibility
Status Completed
Enrollment 90
Est. completion date December 1, 2019
Est. primary completion date December 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - Patients aged between 18 and 55 years. - ASA I-II - BMI 18-25 Exclusion Criteria: - Major surgery

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Yadigar Yilmaz Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary State-Trait Anxiety Inventory questionnaire State-Trait Anxiety Inventory questionnaire is a direct psychological assessment of preoperative anxiety. 20-30 minutes.
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