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Postoperative Effects of Preoperative Anxiety

B

Baskent University

Status

Completed

Conditions

Pain, Postoperative
Anxiety

Treatments

Drug: Tramadol, paracetamol, diclofenac sodium
Other: Visual analog scale, Ramsay's sedation scale
Diagnostic Test: Spielberger's State-Trait Anxiety Inventory

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

42 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female patients aged between 18-65 years old
  • ASA I-II
  • BMI ≥35 kg/m^2

Exclusion criteria

  • 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

Trial design

42 participants in 2 patient groups

Preoperative anxiety level
Treatment:
Diagnostic Test: Spielberger's State-Trait Anxiety Inventory
Postoperative pain and analgesic consumption
Treatment:
Drug: Tramadol, paracetamol, diclofenac sodium
Other: Visual analog scale, Ramsay's sedation scale

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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