Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04372862
Other study ID # ASPB vs ESBP for mastectomy
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2019
Est. completion date July 30, 2020

Study information

Verified date September 2022
Source Suez Canal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, we are comparing two different techniques of plane blocks to control postoperative mastectomy pain serratus anterior plane block and erector spinae plane block, both are done with ultrasonic guidance We are recording the first time of analgesia request postoperatively as a primary outcome


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date July 30, 2020
Est. primary completion date May 30, 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria: - Female patient age 20 to 65 - ASA I, II - Scheduled for mastectomy Exclusion Criteria: - Allergy to local anaesthetics - Infection at the site of performing the block - Morbidly obese patient of body mass index more than 40 kg/m2

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Plane block
Two different plane blocks to control post-mastectomy pain

Locations

Country Name City State
Egypt Suez Canal University Ismailia

Sponsors (1)

Lead Sponsor Collaborator
Suez Canal University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary First time analgesia request The first time the patient ask for analgesia to control postoperative pain Postoperative up to 24 hours
Secondary Total analgesic consumption The total calculated analgesics that were administered to control post operative pain Postoperative up to 24 hours
Secondary visual analogue scale A subjective method to measure pain, where 0=no pain and 10 = worst comprehensible pain Every two hours for 24 hours postoperative