Ignite Creation Date:
2024-05-06 @ 2:52 PM
Last Modification Date:
2024-10-26 @ 1:38 PM
Study NCT ID:
NCT04442568
Status:
UNKNOWN
Last Update Posted:
2020-06-29
First Post:
2020-06-18
Brief Title:
Impact of ERAS in LSG
Sponsor:
Umraniye Education and Research Hospital
Organization:
Umraniye Education and Research Hospital
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
Emergency admissions of the participants within a month after surgery will be recorded
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
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?:
None