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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04204070
Other study ID # 134/200
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 11, 2019
Est. completion date June 11, 2020

Study information

Verified date April 2020
Source Alexandria University
Contact Yasser Mohamed Osman, assistant professor
Phone 01006357996
Email yasseralx@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim of the work:

To compare the use of the Accuro ultrasound and a real time ultrasound guided epidural combined with the acoustic puncture assisted device to perform the epidural anesthesia Secondary aim is to compare the incidence of complications associated with each technique.

Patient's selection:

This study will be performed on 100 pregnant patients scheduled for normal vaginal delivery under epidural analgesia.

The sample size was calculated by taking success rate of conventional LOR to be 98% in the patients; assuming 80% power, with 95% confidence interval (CI) of two techniques and 30% margin of error.

The study protocol will be reviewed and approved by the Ethics Committee of the Alexandria Main University Hospitals.

A written consent will be obtained from all the patients participating in this study.

Complete history will be taken from all the patients and will be subjected to thorough examination and routine laboratory investigations. Patients will be randomly divided into two equal groups using a computer-generated program.

Group I consists of 50 patients scheduled for epidural catheter insertion using the Accuro ultrasound imaging assisted technique.

Group II consists of 50 patients scheduled for epidural catheter insertion using the real time ultrasound guided technique combined with the use of the acoustic puncture assist device (APAD) technique.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date June 11, 2020
Est. primary completion date June 11, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

- pregnant patients scheduled for normal vaginal delivery under epidural analgesia.

Exclusion Criteria:

- • Any contraindication for epidural analgesia

- High risk pregnancy or precious baby.

- Patients not willing for participation.

Study Design


Related Conditions & MeSH terms

  • Two Different Techniques to Perform Epidural Using Ultrasound

Intervention

Procedure:
Accuro
A research coordinator recorded the depth of the EDS from skin, the number of attempts to perform the epidural anesthesia, the repositioning of the epidural needle either in the same space or in different space, the time taken for space localisation (it is defined as time taken in seconds from skin puncture until the successful space localisation).the total time of the procedure ( time measured from the patient is fully draped and in the proper sitting position till the end of insertion of the epidural catheter ) Any complications such as paresthesia during catheter insertion, dural puncture, blood in catheter and root irritation will be recorded
APAD
APAD

Locations

Country Name City State
Egypt Alexandria university Alexandria

Sponsors (1)

Lead Sponsor Collaborator
Alexandria University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary the depth of the EDS from skin, inmm the procedure time
Primary the number of attempts to perform the epidural anesthesia, the repositioning of the epidural needle either in the same space or in different space the number of attempts to perform the epidural anesthesia, the repositioning of the epidural needle either in the same space or in different space the procedure time
Primary , the time taken for space localisation . (it is defined as time taken in seconds from skin puncture until the successful space localisation) the procedure time
Primary the total time of the procedure ( time measured from the patient is fully draped and in the proper sitting position till the end of insertion of the epidural catheter ) the procedure time
Secondary compare the incidence of complications associated with each technique. compare the incidence of complications associated with each technique. the procedure time