Ignite Creation Date:
2024-05-06 @ 3:47 PM
Last Modification Date:
2024-10-26 @ 1:57 PM
Study NCT ID:
NCT04755725
Status:
COMPLETED
Last Update Posted:
2023-12-19
First Post:
2021-02-03
Brief Title:
Epidural Catheter and Surgically Implanted Rectus Sheath Catheter in Management of Postoperative Pain
Sponsor:
Menoufia University
Organization:
Menoufia University
Study Overview
Official Title:
Comparison Between Epidural Catheter and Surgically Implanted Rectus Sheath Catheter in Management of Postoperative Pain Following Laparotomy
Status:
COMPLETED
Status Verified Date:
2023-12
Last Known Status:
None
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:
None
Brief Summary:
One hundred and twenty patients at age range from 18 to 60 undergoing laparotomy was enrolled in this study Patients were randomly assigned to two groups 60 in epidural group and the other 60 patients in rectus catheter group epidural catheter inserted pre induction but rectus sheath catheter inserted by the surgeon at the end of surgery
Detailed Description:
One hundred and twenty patients at age range from 18 to 60 undergoing laparotomy was enrolled in this study Patients were randomly assigned to two groups 60 in epidural group and the other 60 patients in rectus catheter group epidural catheter inserted pre induction but rectus sheath catheter inserted by the surgeon at the end of surgery In both groups we activated with10 ml bupivacain25 before patient recovery then 10 ml bupivacain125 each 6 hours If patient still in pain 1gm perflgan injected If patient still in pain 10 mg nalufine for 70 kg patient injected we will record pulse blood pressure and visual analogue scale at 061224 and 36 hours postoperative Also Occurrence of nausea and vomiting Time of return of bowel movement Time of discharage and amount of analgesia used will be recorded Results discution will be later
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