Viewing Study NCT04445857



Ignite Creation Date: 2024-05-06 @ 2:51 PM
Last Modification Date: 2024-10-26 @ 1:38 PM
Study NCT ID: NCT04445857
Status: COMPLETED
Last Update Posted: 2021-05-27
First Post: 2020-06-21

Brief Title: Efficacy of Coadministration of Calcitonin and Hyperbaric Bupivacaine in Spinal Anesthesia in Tramadol-abuse Patients
Sponsor: Ain Shams University
Organization: Ain Shams University

Study Overview

Official Title: Efficacy of Coadministration of Calcitonin and Hyperbaric Bupivacaine in Spinal Anesthesia in Lower Abdominal and Limb Surgeries in Tramadol-abuse Patients a Randomized Controlled Trial
Status: COMPLETED
Status Verified Date: 2024-07
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: Increasing duration of local anesthetic action is desired for prolongation of postoperative patient comfort as well as decreasing perioperative opioid consumption and subsequent side effects Calcitonin discovered in 1961 has been established synthesized and developed for use in treating disease In 1983 it was demonstrated that calcitonin is an analgesic which is also effective in the epidural and subarachnoid spacesTramadol abuse has dramatically increased in Egypt since 2008 and has led to many admissions to addiction treatment centersIt was shown that the duration of sensory block of spinal anesthesia with hyperbaric bupivacaine in chronic opium abusers undergoing lower extremity orthopedic surgery was much shorter in chronic opium abusers compared with non-abusers
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