NCT03213262

Brief Summary

In this study, investigators wanted to investigate the effect of preoperative anxiety level on anesthesia preference of patient. Before surgery, patients will fill the forms of Pain catastrophising scale (PCS), Beck depression and Beck anxiety scale. After surgery, these forms will be evaluated according to the choice of anesthesia.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
138

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2017

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 7, 2017

Completed
Same day until next milestone

Study Start

First participant enrolled

July 7, 2017

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 11, 2017

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 18, 2017

Completed
6 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 24, 2017

Completed
Last Updated

September 26, 2017

Status Verified

July 1, 2017

Enrollment Period

2 months

First QC Date

July 7, 2017

Last Update Submit

September 25, 2017

Conditions

Anxiety

Outcome Measures

Primary Outcomes (1)

  • Anesthesia preference and anxiety

    The spinal and general anesthesia preference according to the anxiety level of cesarean patients

    one time in three months

Study Arms (2)

General anesthesia

The effect of anxiety on the choice of anesthesia will be evaluated.

spinal anesthesia

Cesarean patients with spinal anesthesia

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Ceserean patients

You may qualify if:

  • Between 18 and 40 years
  • Planned to undergo ceserean
  • An American Society of Anesthesiologists score of 1 or 2

You may not qualify if:

  • Psychiatric diseases
  • Rejected to participation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gaziosmanpasa university

Tokat Province, 60200, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Hakan Tapar

    Gaziosmanpasa university

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assist.Prof.

Study Record Dates

First Submitted

July 7, 2017

First Posted

July 11, 2017

Study Start

July 7, 2017

Primary Completion

September 18, 2017

Study Completion

September 24, 2017

Last Updated

September 26, 2017

Record last verified: 2017-07

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)