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Clinical Trials/NCT05334160
NCT05334160
Completed
Not Applicable

Evaluation of the Postoperative Effects of Preoperative Abdominal Breathing Exercises in Laparoscopic Cholecystectomy Operations

Tokat Gaziosmanpasa University1 site in 1 country70 target enrollmentNovember 15, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Analgesia
Sponsor
Tokat Gaziosmanpasa University
Enrollment
70
Locations
1
Primary Endpoint
NRS
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Postoperative evaluation of patients who did and did not do preoperative abdominal breathing exercises.

Detailed Description

The respiratory type and pattern of all patients will be recorded before gallbladder surgery. In Group P, abdominal breathing training will be given to the patients in this group. They will perform abdominal breathing for at least 5 minutes 6 times a day until surgery. In Group C,patients who are not given abdominal breathing. In the intraoperative period, 10 mg / kg paracetamol and 0.05 mg / kg morphine will be used for postoperative analgesia. After surgery, all patients will be given 10 mg/kg paracetamol every 8 hours and will be fitted with a patient-controlled analgesia (PCA) device (Tramadol HCL). PCA device bolus dose will be set to 20 mg, lock time will be set to 10 minutes and the number of buttons per hour will be set as 3.for postoperative analgesia.After surgery, NRS scores of the patients will be evaluated (in the recovery room, 1,2,6,12 and 24 hours. Preoperative anxiety, postoperative discharge time and analgesic consumption of all patients will be recorded.

Registry
clinicaltrials.gov
Start Date
November 15, 2021
End Date
May 15, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Tokat Gaziosmanpasa University
Responsible Party
Principal Investigator
Principal Investigator

Hakan Tapar

M.D

Tokat Gaziosmanpasa University

Eligibility Criteria

Inclusion Criteria

  • Planned to gall bladder surgery
  • An American Society of Anesthesiologists score of 1,2 or 3

Exclusion Criteria

  • Severe cardiovascular disease
  • Respiratory disease
  • Psychiatric disease
  • Those who have chronic pain

Outcomes

Primary Outcomes

NRS

Time Frame: During postoperative up to 24 hour

Opioid consumption

Time Frame: During postoperative up to 24 hours

Study Sites (1)

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