Viewing Study NCT04442568


Ignite Creation Date: 2025-12-24 @ 6:25 PM
Ignite Modification Date: 2025-12-24 @ 6:25 PM
Study NCT ID: NCT04442568
Status: UNKNOWN
Last Update Posted: 2020-06-29
First Post: 2020-06-18
Is Possible Gene Therapy: False
Has Adverse Events: False

Brief Title: Impact of ERAS in LSG
Sponsor: Umraniye Education and Research Hospital
Organization:

Study Overview

Official Title: Enhanced Recovery After Surgery Protocol in Laparoscopic Sleeve Gastrectomy
Status: UNKNOWN
Status Verified Date: 2020-06
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ERAS-LSG
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.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: