Pre-procedural Anxiety and Sedation.

NCT01958151 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2013-10-09

No results posted yet for this study

Summary

Colonoscopy is an outpatient procedure performed frequently as a screening test for diagnosis and treatment of a wide range of gastrointestinal problems. It is often viewed as an invasive procedure with the potential for embarrassment, discomfort, and worry. Such fears can result in anxiety that may decrease the tolerance and cooperation of the patient, limit the success of the procedure, and increase the likelihood of complications. Therefore, colonoscopy is frequently performed under sedation. The anxiety level of the patient before the procedure may increase the requirement for sedation. It is important for the anesthesiologist to predict the effective dosages of sedation before the procedure to ensure rapid and comfortable sedation as well as prompt recovery and discharge of the patient.

This prospective cohort study is planned to evaluate the effects of pre-procedural anxiety level on the dose of propofol needed for patient and surgeon satisfaction during colonoscopy.

Conditions

Interventions

OTHER

State-Trait Anxiety Inventory Scores

Patients are evaluated before the procedure with State-Trait Anxiety Inventory scores to determine the anxiety level.

Sponsors & Collaborators

  • Basak Ceyda MECO

    lead OTHER

Principal Investigators

  • Basak Ceyda MECO, MD, DESA · Ankara University Faculty of Medicine

  • Mehmet Ayhan Kuzu, Prof · Ankara University Faculty of Medicine

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01958151 on ClinicalTrials.gov