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OpenTrials
Completed

NCT Number: NCT05334160

Pain and Abdominal Breathing Exercises

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

Completed

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Key information

Conditions

Analgesia Agnosia Breathing Nervous System Diseases Neurobehavioral Manifestations Neurologic Manifestations Pathologic Processes Pathological Conditions, Signs and Symptoms Perceptual Disorders Respiration Disorders Respiratory Aspiration Respiratory Tract Diseases Signs and Symptoms

Age range

20 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hakan Tapar

Tokat Province, 60200, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Opioid consumption

    Time frame: During postoperative up to 24 hours

  2. NRS

    Time frame: During postoperative up to 24 hour

Sponsors and collaborators

Lead sponsor

Tokat Gaziosmanpasa University

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Apr 19, 2022
Registry last updated
Oct 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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