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Impact of ERAS in LSG

Enhanced Recovery After Surgery Protocol in Laparoscopic Sleeve Gastrectomy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04442568
Acronym
ERAS-LSG
Enrollment
100
Registered
2020-06-22
Start date
2020-07-01
Completion date
2021-06-01
Last updated
2020-06-29

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

Conditions

Enhanced Recovery After Surgery, Laparoscopic Sleeve Gastrectomy, Nausea, Postoperative, Pain, Postoperative, Vomiting, Postoperative

Brief summary

Patients with BMI \>35 and chronic diseases or BMI \>40 will be scheduled to receive Laparoscopic Sleeve Gastrectomy (LSG). Two groups are planned according to receive Enhance recovery after surgery (ERAS) protocol or not. All participants will receive standard LSG. Participants of ERAS will receive anesthesia and post-surgical nutrition protocol which are determined for ERAS. All patients will be checked for status of pain with VAS score, nausea and vomiting with PONV score at postoperative 2nd hour, 12th hour. In ERAS group liquid oral intake will be started between postoperative 2nd and 4th hours. In no ERAS group liquid oral intake will be started in the morning of postoperative first day. The patients who provides discharge criterias will be discahrged. these criterias are; To provide adequate pain relief with paracetamol and nonsteroidal painkillers, No wound problem, No complications after surgery, Pulse rate \<90 beats / min, temperature ≤ 37 · 5 ° C, respiratory rate, \<20 breaths / minute, To be able to mobilize easily, To be able to drink 1 liter of water after surgery. Emergency admissions of the participants within a month after surgery will be recorded.

Interventions

OTHERERAS

early mobilisation, early oral intake, early discharge

Sponsors

Umraniye Education and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Patients

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* must be performed laparoscopic sleeve gastrectomy * body mass index \> 35 with a comorbidıty or ,body mass index \> 40

Exclusion criteria

* surgery with peroperative complication * revision surgery applications

Design outcomes

Primary

MeasureTime frameDescription
length of hospital staytill discharge, an average of 36 hoursthe time (in hours) from the start of surgery to the discharge of patients in both groups
number of emergency re-admission after surgeryduring postoperative first 30 daysnumber of emergency re-admission after surgery due to complications or patients discomfort
Score of Visual analog scalepostoperative 24 hoursVAS scores that evaluate postoperative pain in both groups will be compared (minimum score 0, maxımum score 10 and higher scores mean a worse outcome)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026