The Effect of Anesthetic Methods on Gastrointestinal Motility

NCT05951686 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2024-08-13

No results posted yet for this study

Summary

The goal of this randomized controlled single blinded study is to compare the effect of the type of anesthesia on gastrointestinal motility in patients scheduled for laparoscopic sleeve gastrectomy. The main question it aims to answer is how do inhalation anesthesia and total intravenous anesthesia effect the gastrointestinal peristalsis during anastomosis.

Participants will be American Society of Anesthesiology (ASA) physical status II and III, between 18- 60 ages.

Researchers will compare inhalation anesthesia where desflurane is used with total intravenous anesthesia to see if the gastrointestinal motility differs between the groups.

Conditions

  • Anesthesia
  • Total Intravenous Anesthesia

Interventions

DRUG

Desflurane

In inhalation group, desflurane will be used for general anesthesia maintenance under the screening with Patient State Index (PSI) between a score of 25-50. Remifentanil infusion is used with desflurane with a dose of 0.05-2 mcg/ kg/ min according to PSI . Fresh gas flow is used 2 L/ min with a mixture of 50%- 50% oxygen and medical air in both groups.

DRUG

Remifentanil infusion

Remifentanil infusion will be used with a dose of 0.05-2 mcg/ kg/ min under the screening with Patient State Index (PSI) between a score of 25-50 in both groups.

OTHER

Fresh gas

Fresh gas flow will be used 2 L/ min with a mixture of 50%- 50% oxygen and medical air in both groups.

DRUG

Propofol infusion

Propofol infusion will be used for general anesthesia maintenance with a dose of under the screening of Patient State Index (PSI) between a score of 25-50 in group tiva.

Sponsors & Collaborators

  • Bozyaka Training and Research Hospital

    lead OTHER

Principal Investigators

  • Halide H Şahinkaya, MD · Izmir Bozyaka Education and Research Hospital

  • Ahmet M Öztürk, MD · Izmir Bozyaka Education and Research Hospital

  • Çağlar Ayar, MD · Izmir Bozyaka Education and Research Hospital

  • Hüseyin Özkarakaş, MD · Izmir Bozyaka Education and Research Hospital

  • Bülent Çalık, Ass. Prof · Izmir Bozyaka Education and Research Hospital

  • Zeki T Tekgül, Ass. Prof. · Izmir Bozyaka Education and Research Hospital

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-15
Primary Completion
2023-10-15
Completion
2023-12-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05951686 on ClinicalTrials.gov