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Clinical Trials/NCT02938845
NCT02938845
Completed
Not Applicable

Factors Related to Patients' Anxiety Before and After Hysterectomy

Zeynep Kamil Maternity and Pediatric Research and Training Hospital1 site in 1 country74 target enrollmentJanuary 2013
ConditionsAnxiety

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety
Sponsor
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Enrollment
74
Locations
1
Primary Endpoint
STAI-S's Inventory
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study was to identify factors that may contribute to anxiety of patients undergoing total abdominal hysterectomy(TAH) or total laparoscopic hysterectomy(TLH) before and after the operation. Thus, we aimed to learn whether anxiety levels change according to the type of hysterectomy.

Detailed Description

Hysterectomy is the most common gynecological procedure worldwide. . There has been a increasing interest towards to more minimally invasive procedures in the past decade. Hysterectomy operation anxiety is a complex phenomenon affected by various parameters. Patients' anxiety may be affected by their age, gender, educational status,type of operation and personality. Each patient's anxiety was measured using Spielberger's State-Trait Anxiety Inventory immediately before, immediately after the operation.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
December 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Responsible Party
Principal Investigator
Principal Investigator

Ahmet Eser

medical doctor

Zeynep Kamil Maternity and Pediatric Research and Training Hospital

Eligibility Criteria

Inclusion Criteria

  • undergone hysterectomies for benign reasons.

Exclusion Criteria

  • malignancy, additional operation beside hysterectomy( such as salpingo-oophorectomy), history of two or more previous caesarean sections, history of previous abdominal surgery, autoimmune disease, coagulation disorders, with known systemic or psychiatric disease, those receiving any regular sedative medication at the time of the procedure

Outcomes

Primary Outcomes

STAI-S's Inventory

Time Frame: change from immediately before operation to immediately after the operation.

STAI-T's Inventory

Time Frame: change from immediately before operation to immediately after the operation.

Study Sites (1)

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