ClinicalTrials.Veeva

Menu

Does Low Flow Anesthesia Reduce Postanaesthetic Emergence Agitation?

S

Sakarya University

Status and phase

Completed
Phase 4

Conditions

Agitated; State, Acute Reaction to Stress

Treatments

Drug: Antiemetics
Drug: Analgesics

Study type

Interventional

Funder types

Other

Identifiers

NCT03862391
Sakarya School of Medicine

Details and patient eligibility

About

In this study, the investigators aimed to compare postanesthetic agitation in patients undergoing laparotomic gynecological surgery under general anesthesia using sevoflurane at a fresh gas flow rate of 2 L / min with fresh gas flow rate of 0.5 L / min.

Full description

Emergence agitation is a temporary state of mental anxiety that occurs during general anesthesia recovery. It is characterized by emergence agitation, hallucination, excitation, delusion and confusion. Increased hemorrhage due to hypertension may cause serious complications such as injury to the surgical site, patients' self-removal of surgical drains and catheters, and self-extubation. Due to these, emergence agitation results need for additional treatment, psychological stress and increased medical workload for patients and their families.

Emergence agitation after general anesthesia in adult patients was reported up to 20%. However, the ratios are very wide.

In our operating room, the investigators observed that patients with low flow anesthesia were less agitated in the recovery phase than patients with normal flow anesthesia. In our researches, the investigators have not found any studies on the agitation values of patients who underwent low flow anesthesia in the literature.

Enrollment

60 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA physical status 1 and 2, underwent gynicological laparotomic surgery under general anesthesia, followed up in PACU(postoperative care unit)

Exclusion criteria

  • ASA 3 or 4, mental retardation, psychiatric disease, history of malignant hyperthermia in patient or her family, neurological disease, morbid obesity, history of asthma and follow-up in the intensive care unit.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Postsurgical Pain
Active Comparator group
Description:
pain is defined as unpleasant sensation that can range from mild, localized discomfort to agony.
Treatment:
Drug: Analgesics
Postanesthesia nausea and vomiting
Active Comparator group
Description:
nausea defined as feeling of sickness or discomfort in the stomach that may come with an urge to vomit.
Treatment:
Drug: Antiemetics

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems