Effects of Different Warming Methods in Laparoscopic Cholecystectomy Surgery

NCT04741815 | Completed

• 1 other identifier: 2018-3/16
• Study Type: interventional
• Target: 123
• Locations: 1 country
• Sites: 1

Brief Summary

Cold gases given during laparoscopic cholecystectomy are the most important cause of hypothermia. However, even surgery alone is an 80% important cause of hypothermia. Inadvertent perioperative hypothermia is a common complication of the surgical process that can cause serious complications. In most of the patients, tremors, increase in pain, deterioration in comfort and changes in some physiological parameters can be seen. Despite this, there are not enough warming devices that nurses can use practically and are easy to use, affordable and comfortable for the patient. In the literature, it is stated in the evidence-based guidelines for determining the hypothermia risks of patients and taking early precautions.

Conditions

Inadvertent Perioperative Hypothermia

Keywords

Inadvertent Perioperative Hypothermia; laparoscopic cholecystectomy; nurse; pain; physiological parameters; shivering; thermal comfort

Outcome Measures

Primary Outcomes (3)

• Pain Visual Analog Scale

  The Visual Pain Scale is a scale of ten centimeters, created to inquire about the pain status of individuals. Zero indicates no pain while ten indicates the most severe pain. This chart is prepared as a blank line for self-evaluation and the prepared chart is read on the ruler.

  It is measured preoperatively and after the end of the operation at the 30th minute, 12th hour and 24th hour (up to 24 hours). Change from baseline Pain Visual Analog Scale scores at 24 hours.

• Thermal Comfort Visual Analog Scale

  Horn et al. It is a visual assessment scale developed by. Thermal comfort is evaluated using a 100 mm long visual benchmark scale. Zero points represent the worst unbearable cold, 50 mm thermal comfort, 100 mm unbearable temperature. Objective responses of the patients were determined by making an evaluation from 0 to 100mm.

  It is measured before surgery and every half hour after surgery (up to 2 hours). The change in thermal comfort score before and within the first two hours after surgery is recorded.

• Body Temperature Scale

  It is the measurement chart prepared by the researcher. Includes measurement of body temperature over time.

  It is measured before surgery and every fifteen minutes after surgery (up to 2 hours). The change in Body Temperature Scale score before and within the first two hours after surgery is recorded.

Secondary Outcomes (3)

• Tremor Rating Scale

  It is measured before and every 15 minutes after surgery (up to 1 hour). Changes in tremor from the first minute to an hour after surgery.

• Hemoglobin Parameters Scale

  The hemoglobin level is measured before surgery and at 24th hours after surgery (up to 24 hours). Change from baseline hemoglobin level scores at 24 hours.

• International Normalized Ratio Parameters Scale

  The Pt INR level is measured before surgery and at 1th hours after surgery (up to 1 hours). Change from preoperative Pt INR level at postoperative 1st hour.

Study Arms (3)

Forced Air Warming Group

EXPERIMENTAL

There is no intervention in patients before the operation. When he comes out of the operation and comes to the post-anesthesia care unit (PACU), he is warmed by forced air. When the body temperature of the patients reaches 36 ° C, they are transferred to the clinic with a cover and blanket.

Device: Forced Air Warming

Peripheral Carbon Fiber Warming Group

EXPERIMENTAL

Gloves and socks developed by the researcher are applied half an hour before the operation. These materials, called environmental warming, have three layers. The first layer in contact with the patient is a thermal inner sheath made of 90% Polyester and 10% Polyamide and is used to maintain body temperature. The second layer consists of carbon fiber warmer and foil. The end of the carbon fiber warmer is USB connected. When the connection is plugged in, the warmer works. The third layer is again made of thermal fabric. A rubber bandage is made to separate the last layer from the external environment and to maintain the patient's body temperature. The USB connection is removed while patients are sent for surgery. After the operation, rewarming is started in the post-anesthesia care unit. When the patient's body temperature reaches 36 ° C, he is transferred to the clinic with a cover and blanket.

Device: Peripheral Carbon Fiber Warming

Control Group

NO INTERVENTION

A routine hospital procedure is applied. The patient is not warmed before going to surgery. A cover and blanket are used passively after being taken to the PACU from the operation.

Interventions

Forced Air Warming DEVICE

It consists of the WarmAir® unit and FilteredFlo® blankets. FilteredFlo® blankets are a cover designed to cover the entire body and extremities with air channels that provide the appropriate distribution of patient warm. The WarmAir® warming device connected to the shroud via a pipe; it has three temperature settings, 32.2 C, 37.8 C, and 43.3 C.

Forced Air Warming Group

Peripheral Carbon Fiber Warming DEVICE

It was developed by the researcher. Designed as gloves and socks, these warming materials have three layers. The first layer in contact with the patient and the third layer in contact with the external environment is a thermal material to maintain body temperature. The second floor consists of a USB-connected carbon fiber warmer and foil.

Peripheral Carbon Fiber Warming Group

Eligibility Criteria

• Age: 18 Years - 64 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Patients are qualified to answer research questions,
• BMI is between 18.5 kg / m2 and 30 kg / m2,
• Not using therapeutic hypothermia in the surgery,
• Not being treated with chronic opioids,
• Operation time is between 60 minutes and 6 hours,
• Having received general anesthesia during the operation,
• Reception of patients with ASA classification I or II,
• Absence of anemia, coagulation problem and peripheral circulatory disease or metabolic disease.

You may not qualify if:

• Intraoperative and postoperative have complications (bleeding, arrest, nausea, vomiting, etc.),
• Conversion of surgery from laparoscopy to open surgery.

Sponsors & Collaborators

• Bozok University: lead
• Ataturk University: collaborator

Study Sites (1)

Yozgat Bozok University Health Sciences Faculty

Yozgat, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Research Asistant

Study Record Dates

• First Submitted: January 27, 2021
• First Posted: February 5, 2021
• Study Start: January 22, 2019
• Primary Completion: March 20, 2021
• Study Completion: April 30, 2021
• Last Updated: March 2, 2022

Record last verified: 2022-02

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)