NCT04432558

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

87
On Track

Trial Health Score

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

Enrollment
42

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2017

Typical duration 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

Study Start

First participant enrolled

April 12, 2017

Completed
3.2 years until next milestone

First Submitted

Initial submission to the registry

June 5, 2020

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 16, 2020

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2020

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2021

Completed
Last Updated

July 21, 2021

Status Verified

July 1, 2021

Enrollment Period

3.7 years

First QC Date

June 5, 2020

Last Update Submit

July 20, 2021

Conditions

Keywords

Preoperative anxiety levelPostoperative painLaparoscopic sleeve gastrectomy

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

Diagnostic Test: Spielberger's State-Trait Anxiety Inventory

Postoperative pain and analgesic consumption

Other: Visual analog scale, Ramsay's sedation scaleDrug: Tramadol, paracetamol, diclofenac sodium

Interventions

Patients will be wanted to fill the Spielberger's State-Trait Anxiety Inventory the night before the surgery.

Preoperative anxiety level

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.

Postoperative pain and analgesic consumption

The analgesic consumption of the patients will be recorded

Postoperative pain and analgesic consumption

Eligibility Criteria

Age18 Years - 65 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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)

Location

Related Publications (28)

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    PMID: 26153780BACKGROUND
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    PMID: 24077858BACKGROUND
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    PMID: 26499321BACKGROUND
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    PMID: 27551421BACKGROUND
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    PMID: 18496304BACKGROUND
  • Kain ZN, Sevarino F, Alexander GM, Pincus S, Mayes LC. Preoperative anxiety and postoperative pain in women undergoing hysterectomy. A repeated-measures design. J Psychosom Res. 2000 Dec;49(6):417-22. doi: 10.1016/s0022-3999(00)00189-6.

    PMID: 11182434BACKGROUND
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    PMID: 15129613BACKGROUND
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    PMID: 12133084BACKGROUND
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    PMID: 12492793BACKGROUND
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    PMID: 14527702BACKGROUND
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    PMID: 25995061BACKGROUND
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    PMID: 14614791BACKGROUND
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    PMID: 11374599BACKGROUND
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    PMID: 12194547BACKGROUND
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    PMID: 20508787BACKGROUND
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    BACKGROUND
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    PMID: 17352896BACKGROUND

MeSH Terms

Conditions

Anxiety DisordersPain, Postoperative

Interventions

TramadolAcetaminophenDiclofenac

Condition Hierarchy (Ancestors)

Mental DisordersPostoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Intervention Hierarchy (Ancestors)

CyclohexanolsHexanolsFatty AlcoholsAlcoholsOrganic ChemicalsDimethylaminesMethylaminesAminesLipidsAcetanilidesAnilidesAmidesAniline CompoundsPhenylacetatesAcids, CarbocyclicCarboxylic Acids

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

Locations