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Does Pre-operative Patients' Education Facilitates Emergence of Anesthesia Following Bariatric Surgery?

Does Pre-operative Patients' Education Facilitates Emergence of Anesthesia Following Bariatric Surgery?

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01946763
Enrollment
80
Registered
2013-09-20
Start date
2013-06-30
Completion date
2014-05-31
Last updated
2013-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Brief summary

The recovery and emergences from anesthesia is a critical phase. Previous studies focused on pharmological and anesthetics techniques to improve the quality of this stage (duration, complications). In this study, our first aim is to test the impact of pre operative education on the post operative recovery for morbidly obese patient underwent laparoscopic bariatric surgery.

Detailed description

The purpose of our study is to compare post operative immediate recovery and emergence for educated and non educated morbidly obese patients underwent laparoscopic bariatric surgery. Elligibles patients are informed and consented by anesthesiologist. Patients are randomized in 2 groups (G1: educated, G2:non-educated) Patient of G1 are educated in OR before starting anesthesia. This education includes : information about anesthesia emergence, recovery and extubation. Anesthesia and education are conducted by the same anesthesiologist. All patients are operated by the same surgeon. All patients receive same balanced general anesthesia protocol. The recovery starts immediately after the end of the procedure, when the patient has BIS ≥90 and TOF≥9. Recovery assessment and data recording is done by a blinded anesthesiologist.

Interventions

BEHAVIORALpre operative education

Patients will be randomized in 2 groups (G1: educated, G2:non-educated) In the operating room and before starting anesthesia G1 will receive a pre operative education about anesthesia emergence, recovery and extubation.

Sponsors

Procare Riaya Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Adults more than 18 years old. * ASA 2. * BMI more than 35. * scheduled for laparoscopic sleeve gastrectomy or gastric bypass surgery.

Exclusion criteria

* Renal impairment. * Hepatic dysfunction. * Alcohol or drug abuse. * Disabling Central nervous or cerebrovascular diseases. * Treatment with opioids or any psychoactive medication. * Inappropriate Mini mental state exam.

Design outcomes

Primary

MeasureTime frame
Quality of anesthesia recovery6 hours

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026