NCT02531477

Brief Summary

Intra-Carotid delivery of propofol.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
5

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2015

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2015

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

July 15, 2015

Completed
1 month until next milestone

First Posted

Study publicly available on registry

August 24, 2015

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2016

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2016

Completed
Last Updated

August 24, 2015

Status Verified

August 1, 2015

Enrollment Period

1 year

First QC Date

July 15, 2015

Last Update Submit

August 21, 2015

Conditions

Anesthesia

Outcome Measures

Primary Outcomes (1)

  • effect on painful stimulus perception on HR measurement

    30 minutes

Study Arms (1)

experimental group

EXPERIMENTAL

Intracarotid injection of propofol to detect efficacy and safety as a novel route for drug delivery

Drug: propofol

Interventions

propofolDRUG

intracarotid propofol as an anesthetic agent

experimental group

Eligibility Criteria

Age10 Weeks - 2 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • experimental animals (rabbits)

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mansoura university

Al Mansurah, Dakahlia Governorate, 62215, Egypt

RECRUITING

MeSH Terms

Interventions

Propofol

Intervention Hierarchy (Ancestors)

PhenolsBenzene DerivativesHydrocarbons, AromaticHydrocarbons, CyclicHydrocarbonsOrganic Chemicals

Central Study Contacts

Alrefaey A Kandeel, MD

CONTACT

00201008158591refa3ey2@yahoo.com

Usama M Elsayed, MD

CONTACT

00201028842265UsamaElsayed20@yahoo.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

July 15, 2015

First Posted

August 24, 2015

Study Start

January 1, 2015

Primary Completion

January 1, 2016

Study Completion

February 1, 2016

Last Updated

August 24, 2015

Record last verified: 2015-08

Locations

EG(1)