Postoperative Effects of Preoperative Anxiety
The Effect of Preoperative Anxiety Level to Postoperative Pain and Analgesic Consumption in Patients Who Had Laparoscopic Sleeve Gastrectomy
1 other identifier
observational
42
1 country
1
Brief Summary
INTRODUCTION Patients who will have obesity surgery have about %48 psychiatric illnesses like anxiety disorder. Studies which analyze the relationship between preoperative anxiety level and postoperative pain had reported conflicting results. The aim of this study is to search the relationship between preoperative anxiety level and postoperative pain and analgesic consumption in patients who had laparoscopic sleeve gastrectomy surgery. MATERIAL AND METHODS Our prospective double-blind study is planned to require 86 female patients aged between 18-65 years old, American Society of Anesthesiologists (ASA) I-II and Body mass index (BMI) ≥40 kg/m\^2. Patients having a psychiatric or neurologic disease, brain damage, using psychiatric medications (antidepressants, anxiolytics) and chronic alcohol, known allergy to medications used in the study protocol, inability to provide informed consent will be excluded. Patients will be wanted to fill the Spielberger's State-Trait Anxiety Inventory the night before the surgery. The analgesic consumption of the patients will be recorded by evaluating the pain with Visual analog scale (VAS) and sedation status with Ramsay's sedation scale in the 1st, 4th, 12th and 24th hour of postoperative period. EXPECTATIONS AND SCIENTIFIC CONTRIBUTIONS More satisfying postoperative analgesia may be provided in this group of patients by determining correlation between preoperative anxiety level and postoperative pain and analgesic consumption in patients who had laparoscopic sleeve gastrectomy. Morbidity rate related with pain may be decreased and patient satisfaction may be increased.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2017
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 12, 2017
CompletedFirst Submitted
Initial submission to the registry
June 5, 2020
CompletedFirst Posted
Study publicly available on registry
June 16, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2021
CompletedJuly 21, 2021
July 1, 2021
3.7 years
June 5, 2020
July 20, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Does Preoperative anxiety level effect postoperative pain?
More satisfying postoperative analgesia may be provided in this group of patients by determining correlation between preoperative anxiety level and postoperative pain and analgesic consumption in patients who had laparoscopic sleeve gastrectomy.Patients will be wanted to fill the Spielberger's State-Trait Anxiety Inventory the night before the surgery. The analgesic consumption of the patients will be recorded by evaluating the pain with Visual analog scale (VAS) and sedation status with Ramsay's sedation scale in the 1st, 4th, 12th and 24th hour of postoperative period.
5 years
Study Arms (2)
Preoperative anxiety level
Postoperative pain and analgesic consumption
Interventions
Patients will be wanted to fill the Spielberger's State-Trait Anxiety Inventory the night before the surgery.
The analgesic consumption of the patients will be recorded by evaluating the pain with VAS (Visual analog scale) and sedation status with Ramsay's sedation scale in the 1st, 4th, 12th and 24th hour of postoperative period.
The analgesic consumption of the patients will be recorded
Eligibility Criteria
Female patients aged between 18-65 years old, ASA I-II, which BMI ≥35 kg/m\^2 and have bariatric surgical indications because of morbid (type III) obesity
You may qualify if:
- Female patients aged between 18-65 years old
- ASA I-II
- BMI ≥35 kg/m\^2
You may not qualify if:
- Having a psychiatric or neurologic disease
- Brain damage
- Using psychiatric medications (antidepressants, anxiolytics) and chronic alcohol
- Known allergy to medications used in the study protocol
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Baskent University Zubeyde Hanim Practice and Research Center
Izmir, Karşıyaka, 35540, Turkey (Türkiye)
Related Publications (28)
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PMID: 17352896BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Medical doctor. Anaesthesia and reanimation specialist
Study Record Dates
First Submitted
June 5, 2020
First Posted
June 16, 2020
Study Start
April 12, 2017
Primary Completion
December 31, 2020
Study Completion
January 30, 2021
Last Updated
July 21, 2021
Record last verified: 2021-07
Data Sharing
- IPD Sharing
- Will not share