Ignite Creation Date:
2024-10-26 @ 3:39 PM
Last Modification Date:
2024-10-26 @ 3:39 PM
Study NCT ID:
NCT06588374
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-02-26
Brief Title:
Hemorrhoidectomy Only Versus Hemorrhoidectomy With Lateral Internal Sphincterotomy
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Effect of Lateral Internal Sphincterotomy During Hemorrhoidectomy a Randomized Clinical Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of this study was to access the comparison of pain and complications after hemorrhoidectomy with or without lateral sphincterotomy
Detailed Description:
Hemorrhoids arise from congestion of anal cushions and characteristically lie in the 3 7 and 11 O clock positions with the patient in lithotomy position The most common complication of open hemorrhoidectomy is postoperative pain caused by spasm of the internal sphincter Lateral internal sphincterotomy is one good technique It reduces pain by reducing spasm of internal anal sphincter which is the main cause of pain The addition of lateral internal sphincterotomy to haemorrhoidectomy resulted in generally lower postoperative anal pressures The long-term outcomes which included anal stenosis and anal fissure were significantly lower after lateral internal sphincterotomy patients with recurrence of hemorrhoids severe pain prolonged constipation or anyone with high sphincter tonicity in the digital rectal examination would be a candidate for manometric evaluation of anal canal pressure These patients with high analcanal pressure confirmed with manometry might receive internal sphincterotomy plus hemorrhoid-ectomy
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None